A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2505n100



Internal ID19012873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30158154..30892100hg38UCSC Ensembl
chr15:30450357..31184303hg19UCSC Ensembl
chr15:28237649..28971595hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38733947
hg19733947
hg18733947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052897, nsv1042355
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, HERC2P10, LOC100288637, LOC101059918, ULK4P1, ULK4P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2505n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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