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nsv5487017

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:27,705

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 206 SVs from 37 studies. See in: genome view    
Submitted genomic129,744,293-129,771,997Question Mark
Overlapping variant regions from other studies: 206 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):129,384,133-129,411,837Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5487017Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7129,744,293129,771,997
nsv5487017RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7129,384,133129,411,837

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17003166duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17003166Submitted genomicNC_000007.14:g.129
744293_129771997du
p
GRCh38 (hg38)NC_000007.14Chr7129,744,293129,771,997
nssv17003166RemappedPerfectNC_000007.13:g.129
384133_129411837du
p
GRCh37.p13First PassNC_000007.13Chr7129,384,133129,411,837

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)
nssv17003166<0.00126404
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