A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205616



Internal ID20772656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160130391..160231380hg38UCSC Ensembl
chr2:160986902..161087891hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38100990
hg19100990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350167
Supporting Variants
Samples
Known GenesITGB6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205616
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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