A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196019



Internal ID20763059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29331409..29411201hg38UCSC Ensembl
chr11:29352956..29432748hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3879793
hg1979793
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447058
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196019
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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