nsv4727946

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,485

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 683 SVs from 86 studies. See in: genome view    
Remapped(Score: Perfect):97,196,594-97,219,078Question Mark
Overlapping variant regions from other studies: 683 SVs from 86 studies. See in: genome view    
Submitted genomic97,862,331-97,884,815Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4727946RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr297,196,59497,219,078
nsv4727946Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr297,862,33197,884,815

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject Phenotype
nssv16253652copy number lossSequencingRead depthBreast cancer
nssv16253650copy number lossSequencingRead depthBreast cancer

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16253652RemappedPerfectNC_000002.12:g.971
96594_97202393del		GRCh38.p12First PassNC_000002.12Chr297,196,59497,202,393
nssv16253650RemappedPerfectNC_000002.12:g.971
96594_97219078del		GRCh38.p12First PassNC_000002.12Chr297,196,59497,219,078
nssv16253652Submitted genomicNC_000002.11:g.978
62331_97868130del		GRCh37 (hg19)NC_000002.11Chr297,862,33197,868,130
nssv16253650Submitted genomicNC_000002.11:g.978
62331_97884815del		GRCh37 (hg19)NC_000002.11Chr297,862,33197,884,815

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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