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nsv5704331

  • 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: 130 SVs from 33 studies. See in: genome view    
Submitted genomic34,240,001-34,240,001Question Mark
Overlapping variant regions from other studies: 130 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):34,261,548-34,261,548Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5704331Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1134,240,00134,240,001
nsv5704331RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1134,261,54834,261,548

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17189518alu insertionSequencingOther
nssv17232601alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17189518Submitted genomicNC_000011.10:g.342
40001_34240002ins2
57
GRCh38 (hg38)NC_000011.10Chr1134,240,00134,240,001
nssv17232601Submitted genomicNC_000011.10:g.342
40001_34240002ins2
80
GRCh38 (hg38)NC_000011.10Chr1134,240,00134,240,001
nssv17189518RemappedPerfectNC_000011.9:g.3426
1548_34261549ins25
7
GRCh37.p13First PassNC_000011.9Chr1134,261,54834,261,548
nssv17232601RemappedPerfectNC_000011.9:g.3426
1548_34261549ins28
0
GRCh37.p13First PassNC_000011.9Chr1134,261,54834,261,548

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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