A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730376



Internal ID154042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3066393..3100097hg38UCSC Ensembl
chr20:3047039..3080743hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3833705
hg1933705
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5524528
Supporting Variants
Samples
Known GenesAVP, OXT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730376
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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