A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209808



Internal ID20776849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4518783..4526248hg38UCSC Ensembl
chr2:4566373..4573838hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg387466
hg197466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340504
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209808
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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