A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465461



Internal ID21123014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95025436..95049299hg38UCSC Ensembl
chr11:94758600..94782463hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3823864
hg1923864
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177382
Samples
Known GenesKDM4E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465461
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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