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nsv4386640

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:47,139

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 328 SVs from 52 studies. See in: genome view    
Remapped(Score: Perfect):56,513,086-56,560,224Question Mark
Overlapping variant regions from other studies: 328 SVs from 52 studies. See in: genome view    
Submitted genomic56,906,870-56,954,008Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4386640RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1256,513,08656,560,224
nsv4386640Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1256,906,87056,954,008

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15652826copy number loss2-1548-003SNP arrayGenotyping27

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15652826RemappedPerfectNC_000012.12:g.(?_
56513086)_(5656022
4_?)del
GRCh38.p12First PassNC_000012.12Chr1256,513,08656,560,224
nssv15652826Submitted genomicNC_000012.11:g.(?_
56906870)_(5695400
8_?)del
GRCh37 (hg19)NC_000012.11Chr1256,906,87056,954,008

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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