A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1741n100



Internal ID22787828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110943780..110989840hg38UCSC Ensembl
chr13:111596127..111642187hg19UCSC Ensembl
chr13:110394128..110440188hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3846061
hg1946061
hg1846061
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045197, nsv1045417
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)dgv1741n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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