A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986107



Internal ID20553147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103070292..103070878hg38UCSC Ensembl
chr11:102941021..102941607hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468237
Supporting Variants
Samples
Known GenesDCUN1D5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986107
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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