A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16913612



Internal ID9815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46189075..46195005hg38UCSC Ensembl
chr2:46416214..46422144hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg385931
hg195931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449144
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16913612
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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