A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16918204



Internal ID12891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112702882..112727074hg38UCSC Ensembl
chr2:113460459..113484651hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3824193
hg1924193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447629
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16918204
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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