A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759519



Internal ID9981664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23680437..23840703hg38UCSC Ensembl
Innerchr7:23720056..23880322hg19UCSC Ensembl
Innerchr7:23686581..23846847hg18UCSC Ensembl
Innerchr7:23493296..23653562hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38160267
hg19160267
hg18160267
hg17160267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758108
SamplesNA07000
Known GenesFAM221A, STK31
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)esv2759519
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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