A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1602n100



Internal ID19011970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18471488..18953751hg38UCSC Ensembl
chr13:19045628..19527891hg19UCSC Ensembl
chr13:17943628..18425891hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38482264
hg19482264
hg18482264
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050546, nsv1051306
Samples
Known GenesANKRD20A9P, LINC00408, LINC00417
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1602n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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