A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759777



Internal ID9635236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97030206..97202715hg38UCSC Ensembl
Innerchr10:98789963..98962472hg19UCSC Ensembl
Innerchr10:98779953..98952462hg18UCSC Ensembl
Innerchr10:98779953..98952462hg17UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38172510
hg19172510
hg18172510
hg17172510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758236
SamplesNA18500
Known GenesARHGAP19-SLIT1, LOC100505540, SLIT1
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)esv2759777
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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