A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1622n100



Internal ID22787709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26459403..26494236hg38UCSC Ensembl
chr13:27033540..27068373hg19UCSC Ensembl
chr13:25931540..25966373hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3834834
hg1934834
hg1834834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036036, nsv1054948
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)dgv1622n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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