A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468885



Internal ID21126438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94389463..94391610hg38UCSC Ensembl
chr11:94122629..94124776hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382148
hg192148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995508
Samples
Known GenesGPR83
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468885
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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