A curated catalogue of human genomic structural variation




Variant Details

Variant: essv19236



Internal ID9617265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84046870..84526690hg38UCSC Ensembl
Innerchr15:84715622..85069921hg19UCSC Ensembl
Innerchr15:82506626..82870925hg18UCSC Ensembl
Innerchr15:82506626..82870925hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38479821
hg19354300
hg18364300
hg17364300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758392
Supporting Variants
SamplesNA10838
Known GenesDNM1P41, EFTUD1P1, GOLGA6L4, GOLGA6L5P, LOC100505679, LOC388152, LOC440300, LOC642423
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)essv19236
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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