A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2503n100



Internal ID19012871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30152061..30641319hg38UCSC Ensembl
chr15:30444264..30933522hg19UCSC Ensembl
chr15:28231556..28720814hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38489259
hg19489259
hg18489259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054676, nsv1051750, nsv1041714, nsv1043182, nsv1037715, nsv1054844, nsv1051421, nsv1048282
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, 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)dgv2503n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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