A curated catalogue of human genomic structural variation




Variant Details

Variant: essv18330



Internal ID9957250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46852290..47689665hg19UCSC Ensembl
Innerchr10:46272296..47159671hg18UCSC Ensembl
Innerchr10:46272296..47159671hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19837376
hg18887376
hg17887376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758217
Supporting Variants
SamplesNA11994
Known GenesAGAP9, ANTXRL, ANTXRLP1, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, FAM35BP, FAM35DP, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
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)essv18330
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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