A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226728



Internal ID20793768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24288590..24635500hg38UCSC Ensembl
chr8:24146103..24493013hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38346911
hg19346911
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432093
Supporting Variants
Samples
Known GenesADAM28, ADAM7, ADAMDEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226728
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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