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nsv5712735

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a HERV 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: 94 SVs from 21 studies. See in: genome view    
Submitted genomic25,588,105-25,588,105Question Mark
Overlapping variant regions from other studies: 94 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):25,914,596-25,914,596Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5712735Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr125,588,10525,588,105
nsv5712735RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr125,914,59625,914,596

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17214482herv insertionSequencingOther
nssv17232609herv insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17214482Submitted genomicNC_000001.11:g.255
88105_25588106ins8
656
GRCh38 (hg38)NC_000001.11Chr125,588,10525,588,105
nssv17232609Submitted genomicNC_000001.11:g.255
88105_25588106ins6
38
GRCh38 (hg38)NC_000001.11Chr125,588,10525,588,105
nssv17214482RemappedPerfectNC_000001.10:g.259
14596_25914597ins8
656
GRCh37.p13First PassNC_000001.10Chr125,914,59625,914,596
nssv17232609RemappedPerfectNC_000001.10:g.259
14596_25914597ins6
38
GRCh37.p13First PassNC_000001.10Chr125,914,59625,914,596

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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