A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210141



Internal ID20777181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8639880..8693148hg38UCSC Ensembl
chr3:8681566..8734834hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3853269
hg1953269
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364744
Supporting Variants
Samples
Known GenesSSUH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210141
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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