A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466690



Internal ID21124243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111525636..111526467hg38UCSC Ensembl
chr11:111396361..111397192hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38832
hg19832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986767
Samples
Known GenesC11orf88
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466690
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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