A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191150



Internal ID20758190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80725121..80743694hg38UCSC Ensembl
chr10:82484877..82503450hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3818574
hg1918574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449155
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191150
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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