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nsv5719726

  • Variant Calls:2
  • 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: 122 SVs from 30 studies. See in: genome view    
Submitted genomic36,431,651-36,431,651Question Mark
Overlapping variant regions from other studies: 122 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):36,897,252-36,897,252Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5719726Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr136,431,65136,431,651
nsv5719726RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr136,897,25236,897,252

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17239442sva insertionSequencingOther
nssv17246201sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17239442Submitted genomicNC_000001.11:g.364
31651_36431652ins7
65
GRCh38 (hg38)NC_000001.11Chr136,431,65136,431,651
nssv17246201Submitted genomicNC_000001.11:g.364
31651_36431652ins7
54
GRCh38 (hg38)NC_000001.11Chr136,431,65136,431,651
nssv17239442RemappedPerfectNC_000001.10:g.368
97252_36897253ins7
65
GRCh37.p13First PassNC_000001.10Chr136,897,25236,897,252
nssv17246201RemappedPerfectNC_000001.10:g.368
97252_36897253ins7
54
GRCh37.p13First PassNC_000001.10Chr136,897,25236,897,252

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.

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