A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16912784



Internal ID9265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:52731656..52943440hg38UCSC Ensembl
chr2:52958794..53170578hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg38211785
hg19211785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437220
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16912784
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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