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nsv5485074

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:78

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 211 SVs from 28 studies. See in: genome view    
Submitted genomic150,833,456-150,833,533Question Mark
Overlapping variant regions from other studies: 211 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):150,530,544-150,530,621Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5485074Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7150,833,456150,833,533
nsv5485074RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7150,530,544150,530,621

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17004850duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17004850Submitted genomicNC_000007.14:g.150
833456_150833533du
p
GRCh38 (hg38)NC_000007.14Chr7150,833,456150,833,533
nssv17004850RemappedPerfectNC_000007.13:g.150
530544_150530621du
p
GRCh37.p13First PassNC_000007.13Chr7150,530,544150,530,621

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)
nssv17004850<0.00116404
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