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nsv5727988

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a SVA 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: 238 SVs from 47 studies. See in: genome view    
Submitted genomic175,103,579-175,103,579Question Mark
Overlapping variant regions from other studies: 240 SVs from 47 studies. See in: genome view    
Remapped(Score: Perfect):175,072,715-175,072,715Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5727988Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1175,103,579175,103,579
nsv5727988RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1175,072,715175,072,715

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17239524sva insertionSequencingOther
nssv17244603sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17239524Submitted genomicNC_000001.11:g.175
103579_175103580in
s1240
GRCh38 (hg38)NC_000001.11Chr1175,103,579175,103,579
nssv17244603Submitted genomicNC_000001.11:g.175
103579_175103580in
s1240
GRCh38 (hg38)NC_000001.11Chr1175,103,579175,103,579
nssv17239524RemappedPerfectNC_000001.10:g.175
072715_175072716in
s1240
GRCh37.p13First PassNC_000001.10Chr1175,072,715175,072,715
nssv17244603RemappedPerfectNC_000001.10:g.175
072715_175072716in
s1240
GRCh37.p13First PassNC_000001.10Chr1175,072,715175,072,715

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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