A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464764



Internal ID21122317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63472025..63476235hg38UCSC Ensembl
chr11:63239497..63243707hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg384211
hg194211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993794
Samples
Known GenesHRASLS5, MIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464764
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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