U.S. flag

An official website of the United States government

nsv5433583

  • 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: 133 SVs from 23 studies. See in: genome view    
Submitted genomic69,248,290-69,248,341Question Mark
Overlapping variant regions from other studies: 133 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):69,642,070-69,642,121Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5433583Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1269,248,29069,248,341
nsv5433583RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1269,642,07069,642,121

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17688867alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17688867Submitted genomicNC_000012.12:g.692
48290_69248341ins2
81
GRCh38 (hg38)NC_000012.12Chr1269,248,29069,248,341
nssv17688867RemappedPerfectNC_000012.11:g.696
42070_69642121ins2
81
GRCh37.p13First PassNC_000012.11Chr1269,642,07069,642,121

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)
nssv17688867<0.00126404
Support Center