A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634329



Internal ID21826376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37844407..37844535hg38UCSC Ensembl
chr20:36472809..36472937hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6048483
Supporting Variants
Samples
Known GenesCTNNBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634329
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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