A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623558



Internal ID21815605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47345710..47345859hg38UCSC Ensembl
chr20:45974454..45974603hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052775
Supporting Variants
Samples
Known GenesZMYND8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623558
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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