A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365233



Internal ID21022786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63929055..63931888hg38UCSC Ensembl
chr3:63914731..63917564hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg382834
hg192834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101468
Samples
Known GenesATXN7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365233
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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