A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422618



Internal ID21080171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8996652..8998895hg38UCSC Ensembl
chr8:8854162..8856405hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382244
hg192244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422618
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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