A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732086



Internal ID155752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34285636..34290328hg38UCSC Ensembl
chr20:32873442..32878134hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg384693
hg194693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516737
Supporting Variants
Samples
Known GenesAHCY
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732086
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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