A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757990



Internal ID9633449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:26755188..26934733hg38UCSC Ensembl
Innerchr5:26755297..26934841hg19UCSC Ensembl
Innerchr5:26791054..26970598hg18UCSC Ensembl
Innerchr5:26791054..26970598hg17UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38179546
hg19179545
hg18179545
hg17179545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759335
Supporting Variantsessv19995
SamplesNA07048
Known GenesCDH9
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)esv2757990
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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