A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4417n54



Internal ID18996593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30089917..30626045hg38UCSC Ensembl
chr15:30382120..30918248hg19UCSC Ensembl
chr15:28169412..28705540hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38536129
hg19536129
hg18536129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568717, nsv568718, nsv568720
Samples
Known GenesCHRFAM7A, DKFZP434L187, GOLGA8H, GOLGA8J, GOLGA8T, LOC101059918, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4417n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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