A curated catalogue of human genomic structural variation




Variant Details

Variant: essv17436



Internal ID9615265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144045427..144278415hg38UCSC Ensembl
Innerchr7:143742520..143975508hg19UCSC Ensembl
Innerchr7:143373453..143606441hg18UCSC Ensembl
Innerchr7:143180168..143413156hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38232989
hg19232989
hg18232989
hg17232989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758138
Supporting Variants
SamplesNA12043
Known GenesARHGEF34P, ARHGEF35, CTAGE4, CTAGE8, OR2A1, OR2A12, OR2A14, OR2A2, OR2A20P, OR2A25, OR2A42, OR2A5, OR2A7, OR2A9P, RNU6-57P
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)essv17436
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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