A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758216



Internal ID9633675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42469683..43014743hg38UCSC Ensembl
Innerchr10:42965131..43510191hg19UCSC Ensembl
Innerchr10:42285137..42830197hg18UCSC Ensembl
Innerchr10:42285137..42830197hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38545061
hg19545061
hg18545061
hg17545061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759746
Supporting Variantsessv413, essv18971, essv3290, essv4747, essv17770
SamplesNA12005, NA10831, NA18971, NA18972, NA18620
Known GenesBMS1, CCNYL2, LINC00839, MIR5100, ZNF33B, ZNF37BP
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)esv2758216
Frequency
Sample Size270
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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