A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759700



Internal ID9981845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:80978421..81087205hg38UCSC Ensembl
Innerchr9:83593336..83702120hg19UCSC Ensembl
Innerchr9:82783156..82891940hg18UCSC Ensembl
Innerchr9:80822890..80931674hg17UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38108785
hg19108785
hg18108785
hg17108785
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758191
SamplesNA18563
Known Genes
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)esv2759700
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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