A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210563



Internal ID20777603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35761501..35804200hg38UCSC Ensembl
chr3:35802993..35845692hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3842700
hg1942700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366711
Supporting Variants
Samples
Known GenesARPP21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210563
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00051


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