A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758610



Internal ID9634069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37559110..37818958hg38UCSC Ensembl
Innerchr7:37598713..37858560hg19UCSC Ensembl
Innerchr7:37565238..37825085hg18UCSC Ensembl
Innerchr7:37371953..37631800hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38259849
hg19259848
hg18259848
hg17259848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759523
Supporting Variantsessv14475
SamplesNA19201
Known GenesGPR141
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)esv2758610
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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