A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731492



Internal ID155158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20715256..20717407hg38UCSC Ensembl
chr20:20695899..20698050hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382152
hg192152
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556084
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731492
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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