A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705782



Internal ID21378058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21932659..21932998hg38UCSC Ensembl
chr2:22155531..22155870hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389606
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705782
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0172414


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