A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759522



Internal ID9634981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:35784616..36080828hg38UCSC Ensembl
Innerchr7:35824226..36120438hg19UCSC Ensembl
Innerchr7:35790751..36086963hg18UCSC Ensembl
Innerchr7:35597466..35893678hg17UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38296213
hg19296213
hg18296213
hg17296213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758111
SamplesNA19131
Known GenesSEPT7
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)esv2759522
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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