A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431110



Internal ID21088663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30754065..30755132hg38UCSC Ensembl
chr8:30611582..30612649hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381068
hg191068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165869
Samples
Known GenesUBXN8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431110
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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