A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179081



Internal ID20746121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62504574..62530771hg38UCSC Ensembl
chr11:62272046..62298243hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3826198
hg1926198
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468171
Supporting Variants
Samples
Known GenesAHNAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179081
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00048


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