A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2514n100



Internal ID19012882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30274687..30638297hg38UCSC Ensembl
chr15:30566890..30930500hg19UCSC Ensembl
chr15:28354182..28717792hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38363611
hg19363611
hg18363611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043559, nsv1047012, nsv1053900, nsv1049177, nsv1040351, nsv1051871, nsv1054935, nsv1051737, nsv1054586, nsv1042386
Samples
Known GenesARHGAP11B, CHRFAM7A, GOLGA8H, 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)dgv2514n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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