A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072395



Internal ID21981628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193362775..193362775hg38UCSC Ensembl
chr3:193080564..193080564hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556663
Samples
Known GenesATP13A5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072395
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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