A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231189



Internal ID20798229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9092072..9098899hg38UCSC Ensembl
chr8:8949582..8956409hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386828
hg196828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430381
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231189
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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