A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523664



Internal ID21848023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19985310..19985528hg38UCSC Ensembl
chr2:20185071..20185289hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987162
Supporting Variants
Samples
Known GenesWDR35
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523664
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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