A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192065



Internal ID20759105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22965951..23222439hg38UCSC Ensembl
chr11:22987497..23243985hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38256489
hg19256489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448368
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192065
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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