A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185201



Internal ID20752241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49382839..49385493hg38UCSC Ensembl
chr10:50590885..50593539hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg382655
hg192655
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450967
Supporting Variants
Samples
Known GenesDRGX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185201
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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