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nsv5508510

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31,116

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 174 SVs from 28 studies. See in: genome view    
Submitted genomic117,325,028-117,356,143Question Mark
Overlapping variant regions from other studies: 174 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):117,195,744-117,226,859Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5508510Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11117,325,028117,356,143
nsv5508510RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11117,195,744117,226,859

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17050419duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17050419Submitted genomicNC_000011.10:g.117
325028_117356143du
p
GRCh38 (hg38)NC_000011.10Chr11117,325,028117,356,143
nssv17050419RemappedPerfectNC_000011.9:g.1171
95744_117226859dup
GRCh37.p13First PassNC_000011.9Chr11117,195,744117,226,859

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)
nssv17050419<0.00116404
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