A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474435



Internal ID21131988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66897313..66904417hg38UCSC Ensembl
chr11:66664784..66671888hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg387105
hg197105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185584
Samples
Known GenesPC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474435
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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