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nsv5711994

  • 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: 109 SVs from 28 studies. See in: genome view    
Submitted genomic17,641,685-17,641,685Question Mark
Overlapping variant regions from other studies: 109 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):17,752,494-17,752,494Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5711994Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1917,641,68517,641,685
nsv5711994RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1917,752,49417,752,494

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17199800alu insertionSequencingOther
nssv17233307alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17199800Submitted genomicNC_000019.10:g.176
41685_17641686ins2
80
GRCh38 (hg38)NC_000019.10Chr1917,641,68517,641,685
nssv17233307Submitted genomicNC_000019.10:g.176
41685_17641686ins2
80
GRCh38 (hg38)NC_000019.10Chr1917,641,68517,641,685
nssv17199800RemappedPerfectNC_000019.9:g.1775
2494_17752495ins28
0
GRCh37.p13First PassNC_000019.9Chr1917,752,49417,752,494
nssv17233307RemappedPerfectNC_000019.9:g.1775
2494_17752495ins28
0
GRCh37.p13First PassNC_000019.9Chr1917,752,49417,752,494

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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