A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443956



Internal ID21101509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2187955..2203542hg38UCSC Ensembl
chr11:2209185..2224772hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3815588
hg1915588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443956
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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