U.S. flag

An official website of the United States government

nsv5496825

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:295

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 108 SVs from 26 studies. See in: genome view    
Submitted genomic34,890,726-34,891,020Question Mark
Overlapping variant regions from other studies: 108 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):35,182,927-35,183,221Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5496825Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1534,890,72634,891,020
nsv5496825RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1535,182,92735,183,221

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17701455duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17701455Submitted genomicNC_000015.10:g.348
90726_34891020dup
GRCh38 (hg38)NC_000015.10Chr1534,890,72634,891,020
nssv17701455RemappedPerfectNC_000015.9:g.3518
2927_35183221dup
GRCh37.p13First PassNC_000015.9Chr1535,182,92735,183,221

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)
nssv17701455<0.00116404
Support Center