A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429837



Internal ID21087390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20676345..20677124hg38UCSC Ensembl
chr8:20533856..20534635hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38780
hg19780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166009
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429837
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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