U.S. flag

An official website of the United States government

nsv5509921

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,591

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 82 SVs from 25 studies. See in: genome view    
Submitted genomic95,294,605-95,303,195Question Mark
Overlapping variant regions from other studies: 82 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):95,760,942-95,769,532Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5509921Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1495,294,60595,303,195
nsv5509921RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1495,760,94295,769,532

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17698635deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17698635Submitted genomicNC_000014.9:g.9529
4605_95303195del
GRCh38 (hg38)NC_000014.9Chr1495,294,60595,303,195
nssv17698635RemappedPerfectNC_000014.8:g.9576
0942_95769532del
GRCh37.p13First PassNC_000014.8Chr1495,760,94295,769,532

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)
nssv17698635<0.00116404
Support Center