A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063165



Internal ID21972398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57578465..57578465hg38UCSC Ensembl
chr3:57564192..57564192hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548062
Samples
Known GenesARF4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063165
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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