A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178079



Internal ID20745119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103075678..103833775hg38UCSC Ensembl
chr11:102946407..103704503hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38758098
hg19758097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456947
Supporting Variants
Samples
Known GenesDCUN1D5, DYNC2H1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178079
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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