A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068816



Internal ID21978049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146337877..146337877hg38UCSC Ensembl
chr3:146055664..146055664hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546380
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068816
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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