A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648600



Internal ID21840647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63888745..63888831hg38UCSC Ensembl
chr20:62520098..62520184hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042132
Supporting Variants
Samples
Known GenesTPD52L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648600
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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