A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6598



Internal ID9966003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:6087758..6258798hg38UCSC Ensembl
InnerchrY:5955799..6126839hg19UCSC Ensembl
InnerchrY:6015799..6186839hg18UCSC Ensembl
InnerchrY:5999160..6170200hg17UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38171041
hg19171041
hg18171041
hg17171041
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758598
Supporting Variants
SamplesNA18621
Known GenesTSPY2, TTTY23, TTTY23B
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)essv6598
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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