A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759554



Internal ID9635013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110883242..111147793hg38UCSC Ensembl
Innerchr7:110523298..110787849hg19UCSC Ensembl
Innerchr7:110310534..110575085hg18UCSC Ensembl
Innerchr7:110117249..110381800hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38264552
hg19264552
hg18264552
hg17264552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758129
SamplesNA18505
Known GenesIMMP2L, LRRN3
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)esv2759554
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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