A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26523



Internal ID15489390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21494129..21549824hg38UCSC Ensembl
OuterchrY:21493705..21550314hg38UCSC Ensembl
InnerchrY:23656015..23711710hg19UCSC Ensembl
OuterchrY:23655591..23712200hg19UCSC Ensembl
InnerchrY:22065403..22121098hg18UCSC Ensembl
OuterchrY:22064979..22121588hg18UCSC Ensembl
InnerchrY:21994140..22049835hg17UCSC Ensembl
OuterchrY:21993716..22050325hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3856610
hg1956610
hg1856610
hg1756610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10026
Supporting Variants
SamplesNA18563
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)nssv26523
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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