A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626822



Internal ID21818869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35014430..35015227hg38UCSC Ensembl
chr20:33602233..33603030hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043320
Supporting Variants
Samples
Known GenesTRPC4AP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626822
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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