A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469718



Internal ID21127271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82915203..82915939hg38UCSC Ensembl
chr11:82626245..82626981hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994030
Samples
Known GenesC11orf82
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469718
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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