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nsv5709876

  • 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: 97 SVs from 21 studies. See in: genome view    
Submitted genomic28,912,071-28,912,071Question Mark
Overlapping variant regions from other studies: 97 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):27,239,089-27,239,089Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5709876Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1728,912,07128,912,071
nsv5709876RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1727,239,08927,239,089

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17199898alu insertionSequencingOther
nssv17214332alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17199898Submitted genomicNC_000017.11:g.289
12071_28912072ins2
57
GRCh38 (hg38)NC_000017.11Chr1728,912,07128,912,071
nssv17214332Submitted genomicNC_000017.11:g.289
12071_28912072ins2
57
GRCh38 (hg38)NC_000017.11Chr1728,912,07128,912,071
nssv17199898RemappedPerfectNC_000017.10:g.272
39089_27239090ins2
57
GRCh37.p13First PassNC_000017.10Chr1727,239,08927,239,089
nssv17214332RemappedPerfectNC_000017.10:g.272
39089_27239090ins2
57
GRCh37.p13First PassNC_000017.10Chr1727,239,08927,239,089

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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