A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205620



Internal ID20772660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216658355..216777448hg38UCSC Ensembl
chr2:217523078..217642171hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38119094
hg19119094
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6342371
Supporting Variants
Samples
Known GenesIGFBP2, IGFBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205620
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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