A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465336



Internal ID21122889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67069495..67070065hg38UCSC Ensembl
chr11:66836966..66837536hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185355
Samples
Known GenesRHOD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465336
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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