A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2500n100



Internal ID19012868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30094196..30641319hg38UCSC Ensembl
chr15:30386399..30933522hg19UCSC Ensembl
chr15:28173691..28720814hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38547124
hg19547124
hg18547124
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051730, nsv1048881, nsv1050595, nsv1052282, nsv1035535
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, GOLGA8J, GOLGA8T, 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)dgv2500n100
Frequency
Sample Size29084
Observed Gain12
Observed Loss23
Observed Complex0
Frequencyn/a


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