A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1723n100



Internal ID22787810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86808989..87061681hg38UCSC Ensembl
chr13:87461244..87713936hg19UCSC Ensembl
chr13:86259245..86511937hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38252693
hg19252693
hg18252693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046278, nsv1044991
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)dgv1723n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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