A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207702



Internal ID20774742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:79375217..79428471hg38UCSC Ensembl
chr2:79602343..79655597hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3853255
hg1953255
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341462
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207702
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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