A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428096



Internal ID21085649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119877977..119882428hg38UCSC Ensembl
chr8:120890217..120894668hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg384452
hg194452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164207
Samples
Known GenesDEPTOR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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