A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3584686



Internal ID18423470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30488460..30807423hg38UCSC Ensembl
Innerchr15:30780663..31099626hg19UCSC Ensembl
Innerchr15:28567955..28886918hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38318964
hg19318964
hg18318964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv20e213
Supporting Variantsessv9837878
SamplesKSM003
Known GenesARHGAP11B, GOLGA8H, LOC100288637, ULK4P1, ULK4P2
MethodSNP array
AnalysisWe applied stringent filtering criteria such that CNV had to be a minimum of 1 kb and span 5 consecutive probes, and be detected by at least 2 out of the 3 algorithms. In addition we excluded CNVs that were on the X and Y-chromosomes, or approximately 300 kb adjacent to the centromeres and telomeres.
PlatformAffymetrix Genome-Wide Human SNP Array 6.0
Comments
ReferenceMokhtar_et_al_2014
Pubmed ID24956385
Accession Number(s)esv3584686
Frequency
Sample Size34
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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