A curated catalogue of human genomic structural variation




Variant Details

Variant: essv23565



Internal ID9622075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:22715965..22881291hg38UCSC Ensembl
Innerchr7:22755584..22920910hg19UCSC Ensembl
Innerchr7:22722109..22887435hg18UCSC Ensembl
Innerchr7:22528824..22694150hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38165327
hg19165327
hg18165327
hg17165327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758609
Supporting Variants
SamplesNA06993
Known GenesIL6, SNORD93, TOMM7
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)essv23565
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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