A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16923759



Internal ID16598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213190336..213190446hg38UCSC Ensembl
chr2:214055060..214055170hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434735
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16923759
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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