A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231613



Internal ID20798653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21943901..21946900hg38UCSC Ensembl
chr8:21801412..21804411hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417021
Supporting Variants
Samples
Known GenesXPO7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231613
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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