A curated catalogue of human genomic structural variation




Variant Details

Variant: essv23856



Internal ID9622398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21451664..22032296hg38UCSC Ensembl
InnerchrY:23613550..24178443hg19UCSC Ensembl
InnerchrY:22022938..22587831hg18UCSC Ensembl
InnerchrY:21951675..22516568hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38580633
hg19564894
hg18564894
hg17564894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758603
Supporting Variants
SamplesNA07022
Known GenesRBMY1A1, RBMY1B, RBMY1D, RBMY1E, TTTY13
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)essv23856
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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