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nsv5484006

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:95,134

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 556 SVs from 64 studies. See in: genome view    
Submitted genomic151,280,443-151,375,576Question Mark
Overlapping variant regions from other studies: 556 SVs from 64 studies. See in: genome view    
Remapped(Score: Perfect):150,977,529-151,072,662Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5484006Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7151,280,443151,375,576
nsv5484006RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7150,977,529151,072,662

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17004872duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17004872Submitted genomicNC_000007.14:g.151
280443_151375576du
p
GRCh38 (hg38)NC_000007.14Chr7151,280,443151,375,576
nssv17004872RemappedPerfectNC_000007.13:g.150
977529_151072662du
p
GRCh37.p13First PassNC_000007.13Chr7150,977,529151,072,662

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)
nssv17004872<0.00116404
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