A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218918



Internal ID20785958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63767901..63831600hg38UCSC Ensembl
chr9:68363635..68427334hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3863700
hg1963700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453900
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218918
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.50088


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