A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223731



Internal ID20790771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61883476..61974128hg38UCSC Ensembl
chr8:62796035..62886687hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3890653
hg1990653
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223731
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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