A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758142



Internal ID9980219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:153696422..154061146hg38UCSC Ensembl
Innerchr7:153393507..153758231hg19UCSC Ensembl
Innerchr7:153024440..153389164hg18UCSC Ensembl
Innerchr7:152831155..153195879hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38364725
hg19364725
hg18364725
hg17364725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759577
Supporting Variantsessv7403, essv6222, essv107, essv1617, essv1838, essv19
SamplesNA18942, NA18991, NA18976, NA18636, NA18968, NA18623
Known GenesDPP6
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)esv2758142
Frequency
Sample Size270
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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