A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211156



Internal ID20778196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35761701..35897500hg38UCSC Ensembl
chr3:35803193..35938992hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38135800
hg19135800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360375
Supporting Variants
Samples
Known GenesARPP21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211156
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00092


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