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nsv5503240

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 162 SVs from 30 studies. See in: genome view    
Submitted genomic22,548,641-22,548,711Question Mark
Overlapping variant regions from other studies: 162 SVs from 30 studies. See in: genome view    
Remapped(Score: Pass):23,017,582-23,017,656Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5503240Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1422,548,64122,548,711
nsv5503240RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1423,017,58223,017,656

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17693911deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17693911Submitted genomicNC_000014.9:g.2254
8641_22548711del
GRCh38 (hg38)NC_000014.9Chr1422,548,64122,548,711
nssv17693911RemappedPassNC_000014.8:g.2301
7582_23017656del
GRCh37.p13First PassNC_000014.8Chr1423,017,58223,017,656

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)
nssv17693911<0.00156404
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