A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167435



Internal ID20734475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35874786..35874915hg38UCSC Ensembl
chr8:35732304..35732433hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422005
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167435
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01232


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