A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1720n100



Internal ID22787807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86397552..86448695hg38UCSC Ensembl
chr13:87049807..87100950hg19UCSC Ensembl
chr13:85847808..85898951hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3851144
hg1951144
hg1851144
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044671, nsv1041124
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)dgv1720n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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