A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101468



Internal ID20668508
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 StatusS
Merged Variantsnsv6365233
Supporting Variants
Samples
Known GenesATXN7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101468
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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