A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986865



Internal ID20553905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113427184..113434994hg38UCSC Ensembl
chr11:113297906..113305716hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg387811
hg197811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461915
Supporting Variants
Samples
Known GenesDRD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986865
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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