A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758131



Internal ID9633590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:112852072..113128573hg38UCSC Ensembl
Innerchr7:112492127..112768628hg19UCSC Ensembl
Innerchr7:112279363..112555864hg18UCSC Ensembl
Innerchr7:112086078..112362579hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38276502
hg19276502
hg18276502
hg17276502
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759556
Supporting Variantsessv12601
SamplesNA19098
Known GenesC7orf60, GPR85, LINC00998
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)esv2758131
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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