A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185077



Internal ID20752117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3174583..3207034hg38UCSC Ensembl
chr11:3195813..3228264hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3832452
hg1932452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450997
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185077
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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