A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1716n100



Internal ID22787803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:81561781..82120651hg38UCSC Ensembl
chr13:82135916..82694786hg19UCSC Ensembl
chr13:81033917..81592787hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38558871
hg19558871
hg18558871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049061, nsv1048165
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)dgv1716n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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