A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229985



Internal ID20797025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53412154..53413637hg38UCSC Ensembl
chr8:54324714..54326197hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg381484
hg191484
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425563
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229985
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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