A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1742n100



Internal ID22787829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111022782..111108961hg38UCSC Ensembl
chr13:111675129..111761308hg19UCSC Ensembl
chr13:110473130..110559309hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3886180
hg1986180
hg1886180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045809, nsv1054144, nsv1050654, nsv1046572, nsv1052731, nsv1043326, nsv1037251, nsv1052115, nsv1035917
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)dgv1742n100
Frequency
Sample Size11257
Observed Gain28
Observed Loss0
Observed Complex0
Frequencyn/a


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