A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185156



Internal ID20752196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84323601..84352300hg38UCSC Ensembl
chr10:86083357..86112056hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3828700
hg1928700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442642
Supporting Variants
Samples
Known GenesCCSER2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185156
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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