A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758178



Internal ID9980255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7175387..7482982hg38UCSC Ensembl
Innerchr9:7175387..7482982hg19UCSC Ensembl
Innerchr9:7165387..7472982hg18UCSC Ensembl
Innerchr9:7165387..7472982hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38307596
hg19307596
hg18307596
hg17307596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759662
Supporting Variantsessv6708
SamplesNA18608
Known GenesKDM4C
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)esv2758178
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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