A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210564



Internal ID20777604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35761601..35902800hg38UCSC Ensembl
chr3:35803093..35944292hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38141200
hg19141200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369120
Supporting Variants
Samples
Known GenesARPP21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210564
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00164


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