A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456484



Internal ID21114037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87323055..87332387hg38UCSC Ensembl
chr11:87034097..87043429hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg389333
hg199333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994939
Samples
Known GenesTMEM135
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456484
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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