A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181894



Internal ID20748934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29761024..30097750hg38UCSC Ensembl
chr11:29782571..30119297hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38336727
hg19336727
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439511
Supporting Variants
Samples
Known GenesKCNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181894
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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