A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3040n100



Internal ID22789127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78997347..79029259hg38UCSC Ensembl
chr16:79031244..79063156hg19UCSC Ensembl
chr16:77588745..77620657hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3831913
hg1931913
hg1831913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061270, nsv1057600
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)dgv3040n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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