A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758753



Internal ID9634212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28855749..29174228hg38UCSC Ensembl
Innerchr19:29346656..29665135hg19UCSC Ensembl
Innerchr19:34038496..34356975hg18UCSC Ensembl
Innerchr19:34038496..34356975hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38318480
hg19318480
hg18318480
hg17318480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758494
SamplesNA10863
Known GenesLINC00906, LOC100505835
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)esv2758753
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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