A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2659n100



Internal ID20154275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90301813..90415770hg38UCSC Ensembl
chr15:90845045..90959002hg19UCSC Ensembl
chr15:88646049..88760006hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38113958
hg19113958
hg18113958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039495, nsv1037551, nsv1043624, nsv1047090, nsv1045337
Samples
Known GenesGABARAPL3, IQGAP1, ZNF774
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2659n100
Frequency
Sample Size29084
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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