A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210801



Internal ID20777841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94647616..94666299hg38UCSC Ensembl
chr3:94366460..94385143hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3818684
hg1918684
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210801
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00025


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