A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428686



Internal ID21086239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33130141..33132151hg38UCSC Ensembl
chr8:32987659..32989669hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382011
hg192011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166598
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428686
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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