A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464826



Internal ID21122379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67053647..67113991hg38UCSC Ensembl
chr11:66821118..66881462hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3860345
hg1960345
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178321
Samples
Known GenesRHOD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464826
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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