A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207259



Internal ID20774300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1421234..1508955hg38UCSC Ensembl
chr2:1425006..1512727hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3887722
hg1987722
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332993
Supporting Variants
Samples
Known GenesTPO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207259
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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