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nsv4380190

  • Variant Calls:32
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:55,058

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 528 SVs from 77 studies. See in: genome view    
Remapped(Score: Pass):97,490,656-97,545,713Question Mark
Overlapping variant regions from other studies: 556 SVs from 76 studies. See in: genome view    
Submitted genomic98,079,569-98,162,176Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4380190RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr297,490,65697,545,713
nsv4380190Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr298,079,56998,162,176

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15612008copy number loss1-0640-003SNP arrayGenotyping19
nssv15613251copy number loss1-0680-003SNP arrayGenotyping24
nssv15615158copy number gain1-0750-003SNP arrayGenotyping20
nssv15621084copy number gain1-0190-001SNP arrayGenotyping23
nssv15621732copy number gain1-1009-003SNP arrayGenotyping22
nssv15629788copy number loss1-0578-003SNP arrayGenotyping24
nssv15631340copy number loss1-0622-003SNP arrayGenotyping22
nssv15636043copy number gain13-0099-001SNP arrayGenotyping20
nssv15636536copy number gain13-0132-002SNP arrayGenotyping26
nssv15637998copy number gain14-0062-001SNP arrayGenotyping19
nssv15638403copy number loss14-0135-002SNP arrayGenotyping16
nssv15638714copy number loss14-0010-004SNP arrayGenotyping15
nssv15656401copy number loss2-1717-003SNP arrayGenotyping17
nssv15658601copy number loss3-0539-000SNP arrayGenotyping18
nssv15659244copy number gain4-0074-002SNP arrayGenotyping20
nssv15661341copy number loss5-0068-001SNP arrayGenotyping17
nssv15661761copy number loss4-0035-003SNP arrayGenotyping25
nssv15666331copy number loss7-0069-003SNP arrayGenotyping21
nssv15680158copy number loss222682SNP arrayGenotyping24
nssv15680696copy number loss215271SNP arrayGenotyping21
nssv15681725copy number lossOCD1009-S_0625-6223-2SNP arrayGenotyping24
nssv15683070copy number loss238146SSNP arrayGenotyping16
nssv15683324copy number lossOCD101-1651SNP arrayGenotyping17
nssv15683451copy number lossOCD124-B_188563SNP arrayGenotyping28
nssv15683601copy number lossOCD130-8961053SNP arrayGenotyping23
nssv15686245copy number lossOCD21-S_896393SNP arrayGenotyping19
nssv15686724copy number lossOCD24-S_896442SNP arrayGenotyping17
nssv15695845copy number loss212972SNP arrayGenotyping20
nssv15696290copy number loss157178SNP arrayGenotyping19
nssv15697839copy number loss194735SNP arrayGenotyping21
nssv15698964copy number loss187369SNP arrayGenotyping17
nssv15701629copy number gain223694SNP arrayGenotyping20

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15612008RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15613251RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15615158RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)dup
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15621084RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)dup
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15621732RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)dup
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15629788RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15631340RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15636043RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)dup
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15636536RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)dup
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15637998RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)dup
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15638403RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15638714RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15656401RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15658601RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15659244RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)dup
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15661341RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15661761RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15666331RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15680158RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15680696RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15681725RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15683070RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15683324RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15683451RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15683601RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15686245RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15686724RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15695845RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15696290RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15697839RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15698964RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)del
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15701629RemappedPassNC_000002.12:g.(?_
97490656)_(9754571
3_?)dup
GRCh38.p12First PassNC_000002.12Chr297,490,65697,545,713
nssv15612008Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15613251Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15615158Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)dup
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15621084Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)dup
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15621732Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)dup
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15629788Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15631340Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15636043Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)dup
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15636536Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)dup
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15637998Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)dup
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15638403Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15638714Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15656401Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15658601Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15659244Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)dup
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15661341Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15661761Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15666331Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15680158Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15680696Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15681725Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15683070Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15683324Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15683451Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15683601Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15686245Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15686724Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15695845Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15696290Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15697839Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15698964Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)del
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176
nssv15701629Submitted genomicNC_000002.11:g.(?_
98079569)_(9816217
6_?)dup
GRCh37 (hg19)NC_000002.11Chr298,079,56998,162,176

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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