A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626690



Internal ID21818737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46509120..46509120hg38UCSC Ensembl
chr20:45137759..45137759hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105103
Supporting Variants
Samples
Known GenesZNF334
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626690
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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