A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222360



Internal ID20789400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37706328..37706816hg38UCSC Ensembl
chr8:37563846..37564334hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422823
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222360
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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