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nsv5531113

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,447

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 168 SVs from 32 studies. See in: genome view    
Submitted genomic50,501,270-50,504,716Question Mark
Overlapping variant regions from other studies: 168 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):50,793,467-50,796,913Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5531113Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1550,501,27050,504,716
nsv5531113RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1550,793,46750,796,913

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17703090deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17703090Submitted genomicNC_000015.10:g.505
01270_50504716del
GRCh38 (hg38)NC_000015.10Chr1550,501,27050,504,716
nssv17703090RemappedPerfectNC_000015.9:g.5079
3467_50796913del
GRCh37.p13First PassNC_000015.9Chr1550,793,46750,796,913

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)
nssv17703090<0.00116404
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