A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23601



Internal ID15485385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21878796..21918252hg38UCSC Ensembl
OuterchrY:21876956..21918651hg38UCSC Ensembl
InnerchrY:24024943..24064399hg19UCSC Ensembl
OuterchrY:24023103..24064798hg19UCSC Ensembl
InnerchrY:22434331..22473787hg18UCSC Ensembl
OuterchrY:22432491..22474186hg18UCSC Ensembl
InnerchrY:22363068..22402524hg17UCSC Ensembl
OuterchrY:22361228..22402923hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3841696
hg1941696
hg1841696
hg1741696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10026
Supporting Variants
SamplesNA12872
Known GenesRBMY1A1, RBMY1B, RBMY1D, RBMY1E
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv23601
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer