A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462851



Internal ID21120404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94508601..94515100hg38UCSC Ensembl
chr11:94241767..94248266hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191984
Samples
Known GenesLOC643037
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462851
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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