A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932416



Internal ID22329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33129839..33130783hg38UCSC Ensembl
chr3:33171331..33172275hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38945
hg19945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439985
Supporting Variants
Samples
Known GenesCRTAP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932416
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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