A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182212



Internal ID20749252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132954138..133398753hg38UCSC Ensembl
chr11:132824033..133268648hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38444616
hg19444616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474797
Supporting Variants
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182212
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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