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nsv5492004

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,693

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 84 SVs from 18 studies. See in: genome view    
Submitted genomic100,517,442-100,523,134Question Mark
Overlapping variant regions from other studies: 84 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):102,277,199-102,282,891Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5492004Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10100,517,442100,523,134
nsv5492004RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10102,277,199102,282,891

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17038477deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17038477Submitted genomicNC_000010.11:g.100
517442_100523134de
l
GRCh38 (hg38)NC_000010.11Chr10100,517,442100,523,134
nssv17038477RemappedPerfectNC_000010.10:g.102
277199_102282891de
l
GRCh37.p13First PassNC_000010.10Chr10102,277,199102,282,891

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)
nssv17038477<0.00116404
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