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nsv5500799

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:256,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 622 SVs from 57 studies. See in: genome view    
Submitted genomic118,346,368-118,602,368Question Mark
Overlapping variant regions from other studies: 622 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):120,105,880-120,361,880Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5500799Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10118,346,368118,602,368
nsv5500799RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10120,105,880120,361,880

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17040796duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17040796Submitted genomicNC_000010.11:g.118
346368_118602368du
p
GRCh38 (hg38)NC_000010.11Chr10118,346,368118,602,368
nssv17040796RemappedPerfectNC_000010.10:g.120
105880_120361880du
p
GRCh37.p13First PassNC_000010.10Chr10120,105,880120,361,880

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)
nssv17040796<0.00116404
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