A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422718



Internal ID21080271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24385025..24385543hg38UCSC Ensembl
chr8:24242538..24243056hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167810
Samples
Known GenesADAMDEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422718
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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