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nsv5694560

  • Variant Calls:1
  • 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: 84 SVs from 22 studies. See in: genome view    
Submitted genomic102,127,035-102,127,035Question Mark
Overlapping variant regions from other studies: 84 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):103,886,792-103,886,792Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5694560Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10102,127,035102,127,035
nsv5694560RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10103,886,792103,886,792

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17189322alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17189322Submitted genomicNC_000010.11:g.102
127035_102127036in
s279
GRCh38 (hg38)NC_000010.11Chr10102,127,035102,127,035
nssv17189322RemappedPerfectNC_000010.10:g.103
886792_103886793in
s279
GRCh37.p13First PassNC_000010.10Chr10103,886,792103,886,792

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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