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nsv6140490

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,754

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 394 SVs from 46 studies. See in: genome view    
Submitted genomic70,156,300-70,168,053Question Mark
Overlapping variant regions from other studies: 394 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):69,452,127-69,463,880Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6140490Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr570,156,30070,168,053
nsv6140490RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr569,452,12769,463,880

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16967452duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16967452Submitted genomicNC_000005.10:g.701
56300_70168053dup
GRCh38 (hg38)NC_000005.10Chr570,156,30070,168,053
nssv16967452RemappedPerfectNC_000005.9:g.6945
2127_69463880dup
GRCh37.p13First PassNC_000005.9Chr569,452,12769,463,880

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)
nssv169674520.021492326
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