A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536398



Internal ID21860753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15923144..15923258hg38UCSC Ensembl
chr2:16063266..16063380hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5986542
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536398
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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