A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464159



Internal ID21121712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111515576..111520043hg38UCSC Ensembl
chr11:111386301..111390768hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg384468
hg194468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986766
Samples
Known GenesC11orf88
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464159
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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