A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2619n100



Internal ID22788706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71330447..71363396hg38UCSC Ensembl
chr15:71622786..71655735hg19UCSC Ensembl
chr15:69409840..69442789hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3832950
hg1932950
hg1832950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036446, nsv1052236
Samples
Known GenesTHSD4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2619n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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