A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931983



Internal ID22049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46919813..46948507hg38UCSC Ensembl
chr3:46961303..46989997hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3828695
hg1928695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442868
Supporting Variants
Samples
Known GenesCCDC12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931983
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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