A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209158



Internal ID20776198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:29109801..29118900hg38UCSC Ensembl
chr2:29332667..29341766hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg389100
hg199100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6347341
Supporting Variants
Samples
Known GenesCLIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209158
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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