A curated catalogue of human genomic structural variation




Variant Details

Variant: essv17571



Internal ID9615415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:10001565..10175375hg38UCSC Ensembl
InnerchrY:9839174..10012984hg19UCSC Ensembl
InnerchrY:10449174..10622984hg18UCSC Ensembl
InnerchrY:10432535..10606345hg17UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38173811
hg19173811
hg18173811
hg17173811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758601
Supporting Variants
SamplesNA12762
Known Genes
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)essv17571
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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