A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233146



Internal ID20800186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27720633..27720979hg38UCSC Ensembl
chr8:27578150..27578496hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421036
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233146
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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