A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14536



Internal ID9612043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100618879..100805979hg38UCSC Ensembl
Innerchr10:102378636..102565736hg19UCSC Ensembl
Innerchr10:102368626..102555726hg18UCSC Ensembl
Innerchr10:102368626..102555726hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38187101
hg19187101
hg18187101
hg17187101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758237, esv2758238
Supporting Variants
SamplesNA19202
Known GenesPAX2
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)essv14536
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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