A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619276



Internal ID21811323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36001449..36001580hg38UCSC Ensembl
chr20:34589371..34589502hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043092
Supporting Variants
Samples
Known GenesCNBD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619276
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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