A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1606n100



Internal ID22787693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18828171..18879318hg38UCSC Ensembl
chr13:19402311..19453458hg19UCSC Ensembl
chr13:18300311..18351458hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg3851148
hg1951148
hg1851148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052531, nsv1050383
Samples
Known GenesANKRD20A9P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1606n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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