A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229579



Internal ID20796619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121390201..121419600hg38UCSC Ensembl
chr8:122402441..122431840hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3829400
hg1929400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428940
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229579
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00131


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