A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455893



Internal ID21113446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63828303..63829225hg38UCSC Ensembl
chr11:63595775..63596697hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38923
hg19923
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455893
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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