A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1692n100



Internal ID22787779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63747736..63855900hg38UCSC Ensembl
chr13:64321869..64430033hg19UCSC Ensembl
chr13:63219870..63328034hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38108165
hg19108165
hg18108165
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036603, nsv1046923, nsv1044100, nsv1046914, nsv1042921, nsv1036453, nsv1048045
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1692n100
Frequency
Sample Size11257
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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