A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758183



Internal ID9980260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28472020..28850776hg38UCSC Ensembl
Innerchr9:28472018..28850774hg19UCSC Ensembl
Innerchr9:28462018..28840774hg18UCSC Ensembl
Innerchr9:28462018..28840774hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38378757
hg19378757
hg18378757
hg17378757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759684
Supporting Variantsessv22968
SamplesNA07357
Known GenesLINGO2
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)esv2758183
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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