A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758124



Internal ID9633583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97846972..98018717hg38UCSC Ensembl
Innerchr7:97476284..97648029hg19UCSC Ensembl
Innerchr7:97314220..97485965hg18UCSC Ensembl
Innerchr7:97120935..97292680hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38171746
hg19171746
hg18171746
hg17171746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759546
Supporting Variantsessv19571
SamplesNA12864
Known GenesASNS, MGC72080, OCM2
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)esv2758124
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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