A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165867



Internal ID20732907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30750712..30759874hg38UCSC Ensembl
chr8:30608229..30617391hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg389163
hg199163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416001
Supporting Variants
Samples
Known GenesUBXN8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165867
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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