A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461132



Internal ID21118685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68265957..68280114hg38UCSC Ensembl
chr11:68033425..68047582hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3814158
hg1914158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993560
Samples
Known GenesC11orf24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461132
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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