A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177382



Internal ID20744422
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 StatusS
Merged Variantsnsv6465461
Supporting Variants
Samples
Known GenesKDM4E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177382
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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