U.S. flag

An official website of the United States government

nsv5456336

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:460

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 110 SVs from 23 studies. See in: genome view    
Submitted genomic67,511,384-67,511,843Question Mark
Overlapping variant regions from other studies: 110 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):68,377,102-68,377,561Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5456336Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr467,511,38467,511,843
nsv5456336RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,377,10268,377,561

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16949490deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16949490Submitted genomicNC_000004.12:g.675
11384_67511843del
GRCh38 (hg38)NC_000004.12Chr467,511,38467,511,843
nssv16949490RemappedPerfectNC_000004.11:g.683
77102_68377561del
GRCh37.p13First PassNC_000004.11Chr468,377,10268,377,561

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)
nssv16949490<0.00116404
Support Center