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nsv5710816

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a Alu 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: 139 SVs from 25 studies. See in: genome view    
Submitted genomic35,824,149-35,824,149Question Mark
Overlapping variant regions from other studies: 139 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):34,412,071-34,412,071Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5710816Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2035,824,14935,824,149
nsv5710816RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2034,412,07134,412,071

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17203217alu insertionSequencingOther
nssv17219496alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17203217Submitted genomicNC_000020.11:g.358
24149_35824150ins2
81
GRCh38 (hg38)NC_000020.11Chr2035,824,14935,824,149
nssv17219496Submitted genomicNC_000020.11:g.358
24149_35824150ins2
81
GRCh38 (hg38)NC_000020.11Chr2035,824,14935,824,149
nssv17203217RemappedPerfectNC_000020.10:g.344
12071_34412072ins2
81
GRCh37.p13First PassNC_000020.10Chr2034,412,07134,412,071
nssv17219496RemappedPerfectNC_000020.10:g.344
12071_34412072ins2
81
GRCh37.p13First PassNC_000020.10Chr2034,412,07134,412,071

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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