A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6973



Internal ID9628832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32111710..32495877hg38UCSC Ensembl
Innerchr15:32403911..32788078hg19UCSC Ensembl
Innerchr15:30191203..30575370hg18UCSC Ensembl
Innerchr15:30191203..30575370hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38384168
hg19384168
hg18384168
hg17384168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758375
Supporting Variants
SamplesNA18582
Known GenesCHRNA7, GOLGA8K, GOLGA8O, ULK4P1, ULK4P2, ULK4P3
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)essv6973
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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