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nsv4371390

  • Variant Calls:37
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,765,645

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 7309 SVs from 131 studies. See in: genome view    
Remapped(Score: Pass):46,157,935-47,923,579Question Mark
Overlapping variant regions from other studies: 5448 SVs from 124 studies. See in: genome view    
Submitted genomic46,966,534-48,174,779Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4371390RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1046,157,93547,923,579
nsv4371390Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr1046,966,53448,174,779

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15612460copy number gain1-0671-003SNP arrayGenotyping14
nssv15621260copy number gain1-0989-004SNP arrayGenotyping15
nssv15623145copy number gain1-1060-003SNP arrayGenotyping26
nssv15623526copy number gain1-0269-001SNP arrayGenotyping16
nssv15631985copy number gain1-1063-003SNP arrayGenotyping30
nssv15633990copy number gain11-0021-001SNP arrayGenotyping27
nssv15637112copy number gain12-4676-001SNP arrayGenotyping24
nssv15640196copy number gain14-0119-004SNP arrayGenotyping18
nssv15643292copy number gain14-0364-001SNP arrayGenotyping22
nssv15643344copy number gain14-0364-004SNP arrayGenotyping22
nssv15644954copy number gain2-0270-003SNP arrayGenotyping20
nssv15644976copy number gain2-0270-004SNP arrayGenotyping13
nssv15646495copy number gain2-1189-003SNP arrayGenotyping24
nssv15648768copy number gain2-1285-003SNP arrayGenotyping26
nssv15649686copy number gain2-1329-002SNP arrayGenotyping14
nssv15651328copy number gain2-1371-002SNP arrayGenotyping18
nssv15656001copy number gain3-0526-000SNP arrayGenotyping17
nssv15658200copy number loss3-0646-000SNP arrayGenotyping15
nssv15663864copy number gain5-0140-002SNP arrayGenotyping24
nssv15668138copy number gain7-0207-003SNP arrayGenotyping27
nssv15677351copy number gain242269SSNP arrayGenotyping26
nssv15678012copy number gain241962SSNP arrayGenotyping24
nssv15678799copy number gain174227SNP arrayGenotyping12
nssv15678893copy number gain183433SNP arrayGenotyping27
nssv15679807copy number gain208585SNP arrayGenotyping15
nssv15680586copy number gain215105SNP arrayGenotyping32
nssv15682346copy number gainOCD110-B_1654SNP arrayGenotyping23
nssv15687740copy number gainOCD18-S_896352SNP arrayGenotyping20
nssv15695996copy number gain160878SNP arrayGenotyping17
nssv15696095copy number gain155473SNP arrayGenotyping18
nssv15697942copy number gain216640SNP arrayGenotyping17
nssv15698828copy number gain170926SNP arrayGenotyping21
nssv15699534copy number loss156227SNP arrayGenotyping29
nssv15700737copy number gain180793SNP arrayGenotyping15
nssv15702223copy number gain199156SNP arrayGenotyping15
nssv15702238copy number gain223142SNP arrayGenotyping18
nssv15702257copy number gain218211SNP arrayGenotyping13

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15612460RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15621260RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15623145RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15623526RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15631985RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15633990RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15637112RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15640196RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15643292RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15643344RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15644954RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15644976RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15646495RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15648768RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15649686RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15651328RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15656001RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15658200RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)del
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15663864RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15668138RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15677351RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15678012RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15678799RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15678893RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15679807RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15680586RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15682346RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15687740RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15695996RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15696095RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15697942RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15698828RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15699534RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)del
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15700737RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15702223RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15702238RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15702257RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
nssv15612460Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15621260Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15623145Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15623526Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15631985Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15633990Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15637112Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15640196Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15643292Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15643344Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15644954Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15644976Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15646495Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15648768Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15649686Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15651328Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15656001Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15658200Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)del
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15663864Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15668138Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15677351Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15678012Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15678799Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15678893Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15679807Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15680586Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15682346Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15687740Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15695996Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15696095Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15697942Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15698828Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15699534Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)del
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15700737Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15702223Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15702238Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779
nssv15702257Submitted genomicNC_000010.10:g.(?_
46966534)_(4817477
9_?)dup
GRCh37 (hg19)NC_000010.10Chr1046,966,53448,174,779

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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