A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234697



Internal ID20801737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28368853..28376265hg38UCSC Ensembl
chr8:28226370..28233782hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg387413
hg197413
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430385
Supporting Variants
Samples
Known GenesZNF395
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234697
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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