A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733176



Internal ID156842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:55586222..55586262hg38UCSC Ensembl
chr20:54161280..54161320hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549774
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733176
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.11932


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