A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2995



Internal ID9971315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30525683..30860288hg38UCSC Ensembl
Innerchr15:30817886..31152491hg19UCSC Ensembl
Innerchr15:28605178..28939783hg18UCSC Ensembl
Innerchr15:28605178..28939783hg17UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38334606
hg19334606
hg18334606
hg17334606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758374
Supporting Variants
SamplesNA18981
Known GenesARHGAP11B, GOLGA8H, HERC2P10, LOC100288637, ULK4P1, ULK4P2
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)essv2995
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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