U.S. flag

An official website of the United States government

nsv5416763

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 98 SVs from 17 studies. See in: genome view    
Submitted genomic113,364,564-113,364,615Question Mark
Overlapping variant regions from other studies: 96 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):113,235,286-113,235,337Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5416763Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11113,364,564113,364,615
nsv5416763RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11113,235,286113,235,337

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17052448alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17052448Submitted genomicNC_000011.10:g.113
364564_113364615in
s280
GRCh38 (hg38)NC_000011.10Chr11113,364,564113,364,615
nssv17052448RemappedPerfectNC_000011.9:g.1132
35286_113235337ins
280
GRCh37.p13First PassNC_000011.9Chr11113,235,286113,235,337

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)
nssv17052448<0.00116404
Support Center