A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1719n100



Internal ID22787806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85309748..85336715hg38UCSC Ensembl
chr13:85883883..85910850hg19UCSC Ensembl
chr13:84781884..84808851hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3826968
hg1926968
hg1826968
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050860, nsv1043283
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)dgv1719n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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