A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3037n100



Internal ID22789124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78351092..78416213hg38UCSC Ensembl
chr16:78384989..78450110hg19UCSC Ensembl
chr16:76942490..77007611hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3865122
hg1965122
hg1865122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064705, nsv1059159
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)dgv3037n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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