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nsv3957761

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:214,827

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 817 SVs from 73 studies. See in: genome view    
Submitted genomic161,977,841-162,192,667Question Mark
Overlapping variant regions from other studies: 817 SVs from 73 studies. See in: genome view    
Remapped(Score: Perfect):161,695,629-161,910,455Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv3957761Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3161,977,841162,192,667
nsv3957761RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3161,695,629161,910,455

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15218470deletionOptical mappingOptical mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv15218470Submitted genomicNC_000003.12:g.(16
1977841_?)_(?_1621
92667)del
GRCh38 (hg38)NC_000003.12Chr3161,977,841162,192,667
nssv15218470RemappedPerfectNC_000003.11:g.(16
1695629_?)_(?_1619
10455)del
GRCh37.p13First PassNC_000003.11Chr3161,695,629161,910,455

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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