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nsv5720103

  • 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: 432 SVs from 22 studies. See in: genome view    
Submitted genomic103,713,564-103,713,564Question Mark
Overlapping variant regions from other studies: 432 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):102,968,492-102,968,492Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5720103Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX103,713,564103,713,564
nsv5720103RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX102,968,492102,968,492

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17203464alu insertionSequencingOther
nssv17213486alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17203464Submitted genomicNC_000023.11:g.103
713564_103713565in
s279
GRCh38 (hg38)NC_000023.11ChrX103,713,564103,713,564
nssv17213486Submitted genomicNC_000023.11:g.103
713564_103713565in
s234
GRCh38 (hg38)NC_000023.11ChrX103,713,564103,713,564
nssv17203464RemappedPerfectNC_000023.10:g.102
968492_102968493in
s279
GRCh37.p13First PassNC_000023.10ChrX102,968,492102,968,492
nssv17213486RemappedPerfectNC_000023.10:g.102
968492_102968493in
s234
GRCh37.p13First PassNC_000023.10ChrX102,968,492102,968,492

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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