A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759562



Internal ID9981707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:126854735..127037789hg38UCSC Ensembl
Innerchr7:126494789..126677843hg19UCSC Ensembl
Innerchr7:126282025..126465079hg18UCSC Ensembl
Innerchr7:126088740..126271794hg17UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38183055
hg19183055
hg18183055
hg17183055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758132
SamplesNA11840
Known GenesGRM8
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)esv2759562
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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