U.S. flag

An official website of the United States government

nsv5494822

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,062

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 87 SVs from 25 studies. See in: genome view    
Submitted genomic69,894,020-69,900,081Question Mark
Overlapping variant regions from other studies: 87 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):70,360,737-70,366,798Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5494822Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1469,894,02069,900,081
nsv5494822RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1470,360,73770,366,798

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17697857deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17697857Submitted genomicNC_000014.9:g.6989
4020_69900081del
GRCh38 (hg38)NC_000014.9Chr1469,894,02069,900,081
nssv17697857RemappedPerfectNC_000014.8:g.7036
0737_70366798del
GRCh37.p13First PassNC_000014.8Chr1470,360,73770,366,798

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)
nssv17697857<0.00116404
Support Center