A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2502n100



Internal ID20154118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30152061..30529543hg38UCSC Ensembl
chr15:30444264..30821746hg19UCSC Ensembl
chr15:28231556..28609038hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38377483
hg19377483
hg18377483
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049228, nsv1042887, nsv1049267, nsv1053477, nsv1051358, nsv1050200, nsv1053426, nsv1038635, nsv1036631, nsv1039443, nsv1047149, nsv1054072, nsv1038913
Samples
Known GenesCHRFAM7A, DKFZP434L187, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2502n100
Frequency
Sample Size29084
Observed Gain34
Observed Loss95
Observed Complex0
Frequencyn/a


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