A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207640



Internal ID20774680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:128061628..128072743hg38UCSC Ensembl
chr2:128819202..128830317hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3811116
hg1911116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6342823
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207640
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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