A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13613



Internal ID9611018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86866859..87445609hg38UCSC Ensembl
Innerchr10:88626616..89205366hg19UCSC Ensembl
Innerchr10:88616596..89195346hg18UCSC Ensembl
Innerchr10:88616596..89195346hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38578751
hg19578751
hg18578751
hg17578751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758234
Supporting Variants
SamplesNA19127
Known GenesADIRF, AGAP11, BMPR1A, FAM25A, FAM35A, GLUD1, LINC00864, LOC439994, 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)essv13613
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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