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nsv4253252

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,274

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 26 SVs from 11 studies. See in: genome view    
Remapped(Score: Perfect):40,682,892-40,699,165Question Mark
Overlapping variant regions from other studies: 24 SVs from 11 studies. See in: genome view    
Submitted genomic38,839,144-38,855,417Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4253252RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1740,682,89240,699,165
nsv4253252Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1738,839,14438,855,417

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15957885duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15957885RemappedPerfectNC_000017.11:g.406
82892_40699165dup
GRCh38.p12First PassNC_000017.11Chr1740,682,89240,699,165
nssv15957885Submitted genomicNC_000017.10:g.388
39144_38855417dup
GRCh37.p13NC_000017.10Chr1738,839,14438,855,417

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)
nssv159578854.6e-005121694
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