A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1689n100



Internal ID22787776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63727459..63845410hg38UCSC Ensembl
chr13:64301592..64419543hg19UCSC Ensembl
chr13:63199593..63317544hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38117952
hg19117952
hg18117952
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052360, nsv1038263, nsv1042787, nsv1053812
Samples
Known GenesLINC00395, OR7E156P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1689n100
Frequency
Sample Size11257
Observed Gain21
Observed Loss30
Observed Complex0
Frequencyn/a


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