A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208068



Internal ID20775108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202967181..202991875hg38UCSC Ensembl
chr2:203831904..203856598hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg3824695
hg1924695
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340072
Supporting Variants
Samples
Known GenesCARF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208068
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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