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nsv4132870

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,446,708

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2662 SVs from 23 studies. See in: genome view    
Remapped(Score: Good):63,031,275-65,477,982Question Mark
Overlapping variant regions from other studies: 2672 SVs from 23 studies. See in: genome view    
Submitted genomic62,491,653-64,942,895Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4132870RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr763,031,27565,477,982
nsv4132870Submitted genomicGRCh37.p13Primary AssemblyNC_000007.13Chr762,491,65364,942,895

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15920704deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15920704RemappedGoodNC_000007.14:g.630
31275_65477982del
GRCh38.p12First PassNC_000007.14Chr763,031,27565,477,982
nssv15920704Submitted genomicNC_000007.13:g.624
91653_64942895del
GRCh37.p13NC_000007.13Chr762,491,65364,942,895

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv159207044.6e-005121548
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