A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931678



Internal ID21858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44176791..44201094hg38UCSC Ensembl
chr3:44218283..44242586hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3824304
hg1924304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453413
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931678
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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