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nsv5705590

  • 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: 93 SVs from 24 studies. See in: genome view    
Submitted genomic68,990,912-68,990,912Question Mark
Overlapping variant regions from other studies: 93 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):70,750,668-70,750,668Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5705590Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1068,990,91268,990,912
nsv5705590RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1070,750,66870,750,668

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17188637alu insertionSequencingOther
nssv17216537alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17188637Submitted genomicNC_000010.11:g.689
90912_68990913ins1
20
GRCh38 (hg38)NC_000010.11Chr1068,990,91268,990,912
nssv17216537Submitted genomicNC_000010.11:g.689
90912_68990913ins1
20
GRCh38 (hg38)NC_000010.11Chr1068,990,91268,990,912
nssv17188637RemappedPerfectNC_000010.10:g.707
50668_70750669ins1
20
GRCh37.p13First PassNC_000010.10Chr1070,750,66870,750,668
nssv17216537RemappedPerfectNC_000010.10:g.707
50668_70750669ins1
20
GRCh37.p13First PassNC_000010.10Chr1070,750,66870,750,668

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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