U.S. flag

An official website of the United States government

nsv5727618

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a SVA mobile element relative to the reference
  • Publication(s):Chuang et al. 2021

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 112 SVs from 27 studies. See in: genome view    
Submitted genomic56,266,587-56,266,587Question Mark
Overlapping variant regions from other studies: 112 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):56,660,371-56,660,371Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5727618Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1256,266,58756,266,587
nsv5727618RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1256,660,37156,660,371

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17248001sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17248001Submitted genomicNC_000012.12:g.562
66587_56266588ins1
240
GRCh38 (hg38)NC_000012.12Chr1256,266,58756,266,587
nssv17248001RemappedPerfectNC_000012.11:g.566
60371_56660372ins1
240
GRCh37.p13First PassNC_000012.11Chr1256,660,37156,660,371

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

Support Center