A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2495n100



Internal ID19012863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30077711..30644082hg38UCSC Ensembl
chr15:30369914..30936285hg19UCSC Ensembl
chr15:28157206..28723577hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38566372
hg19566372
hg18566372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050658, nsv1040604, nsv1044368, nsv1039789, nsv1042426
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)dgv2495n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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