A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059159



Internal ID19148378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78351092..78405706hg38UCSC Ensembl
Innerchr16:78384989..78439603hg19UCSC Ensembl
Innerchr16:76942490..76997104hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3854615
hg1954615
hg1854615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3037n100
Supporting Variantsnssv3719069
Samples
Known GenesWWOX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059159
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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