A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932461



Internal ID22356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33744807..33748718hg38UCSC Ensembl
chr3:33786299..33790210hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg383912
hg193912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442814
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932461
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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