A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16913764



Internal ID9922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:52166281..52230868hg38UCSC Ensembl
chr2:52393419..52458006hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3864588
hg1964588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440608
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16913764
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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