A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596812



Internal ID21788855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85906769..85906995hg38UCSC Ensembl
chr11:85617812..85618038hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038783
Supporting Variants
Samples
Known GenesCCDC83
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596812
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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