A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462716



Internal ID21120269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133403384..133403965hg38UCSC Ensembl
chr11:133273279..133273860hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988120
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462716
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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