A curated catalogue of human genomic structural variation




Variant Details

Variant: essv24846



Internal ID9623498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86866859..87550005hg38UCSC Ensembl
Innerchr10:88626616..89309762hg19UCSC Ensembl
Innerchr10:88616596..89299742hg18UCSC Ensembl
Innerchr10:88616596..89299742hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38683147
hg19683147
hg18683147
hg17683147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758234
Supporting Variants
SamplesNA07000
Known GenesADIRF, AGAP11, BMPR1A, FAM25A, FAM35A, GLUD1, LINC00864, LOC439994, MINPP1, MIR4678, MMRN2, NUTM2A, NUTM2A-AS1, NUTM2D, SNCG
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)essv24846
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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