A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435388



Internal ID21092941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30764889..30771220hg38UCSC Ensembl
chr8:30622405..30628736hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg386332
hg196332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165872
Samples
Known GenesUBXN8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435388
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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