A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758907



Internal ID9634366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:18512940..18843178hg38UCSC Ensembl
InnerchrY:20674826..21005064hg19UCSC Ensembl
InnerchrY:19134214..19464452hg18UCSC Ensembl
InnerchrY:19062951..19393189hg17UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg38330239
hg19330239
hg18330239
hg17330239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758602
SamplesNA12814
Known GenesHSFY1, HSFY2, TTTY9A, TTTY9B
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)esv2758907
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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