U.S. flag

An official website of the United States government

nsv5502346

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,506

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 158 SVs from 31 studies. See in: genome view    
Submitted genomic69,353,735-69,363,240Question Mark
Overlapping variant regions from other studies: 158 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):69,747,515-69,757,020Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5502346Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1269,353,73569,363,240
nsv5502346RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1269,747,51569,757,020

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17688875duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17688875Submitted genomicNC_000012.12:g.693
53735_69363240dup
GRCh38 (hg38)NC_000012.12Chr1269,353,73569,363,240
nssv17688875RemappedPerfectNC_000012.11:g.697
47515_69757020dup
GRCh37.p13First PassNC_000012.11Chr1269,747,51569,757,020

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)
nssv17688875<0.00166404
Support Center