A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1869n100



Internal ID20153485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35245293..35318983hg38UCSC Ensembl
chr14:35714499..35788189hg19UCSC Ensembl
chr14:34784250..34857940hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3873691
hg1973691
hg1873691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045288, nsv1038396
Samples
Known GenesKIAA0391, PSMA6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1869n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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