A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181881



Internal ID20748921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85864472..86045913hg38UCSC Ensembl
chr11:85575515..85756955hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38181442
hg19181441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475333
Supporting Variants
Samples
Known GenesCCDC83, PICALM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181881
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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