A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208302



Internal ID20775342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202334049..202362566hg38UCSC Ensembl
chr2:203198772..203227289hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3828518
hg1928518
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6339653
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208302
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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