A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2496n100



Internal ID20154112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30077711..30807411hg38UCSC Ensembl
chr15:30369914..31099614hg19UCSC Ensembl
chr15:28157206..28886906hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38729701
hg19729701
hg18729701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044253, nsv1039392, nsv1041754, nsv1045597, nsv1053894, nsv1039647, nsv1053277, nsv1043933, nsv1038766, nsv1039382
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, GOLGA8J, GOLGA8T, LOC100288637, LOC101059918, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2496n100
Frequency
Sample Size29084
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer