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nsv5521152

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:55

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 119 SVs from 21 studies. See in: genome view    
Submitted genomic44,635,941-44,635,995Question Mark
Overlapping variant regions from other studies: 119 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):43,264,582-43,264,636Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5521152Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2044,635,94144,635,995
nsv5521152RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2043,264,58243,264,636

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732559deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732559Submitted genomicNC_000020.11:g.446
35941_44635995del
GRCh38 (hg38)NC_000020.11Chr2044,635,94144,635,995
nssv17732559RemappedPerfectNC_000020.10:g.432
64582_43264636del
GRCh37.p13First PassNC_000020.10Chr2043,264,58243,264,636

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)
nssv17732559<0.00156404
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