A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434766



Internal ID21092319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24328363..24359258hg38UCSC Ensembl
chr8:24185876..24216771hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3830896
hg1930896
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234609
Samples
Known GenesADAM28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434766
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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