A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069824



Internal ID21979057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196564200..196564200hg38UCSC Ensembl
chr3:196291071..196291071hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546353
Samples
Known GenesWDR53
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069824
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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