A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10026



Internal ID15498303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:21491074..21926287hg38UCSC Ensembl
OuterchrY:23652960..24072434hg19UCSC Ensembl
OuterchrY:22062348..22481822hg18UCSC Ensembl
OuterchrY:21991085..22410559hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38435214
hg19419475
hg18419475
hg17419475
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26537, nssv26091, nssv27903, nssv28324, nssv27641, nssv25630, nssv26523, nssv25607, nssv27603, nssv23573, nssv23601, nssv28322, nssv26110
SamplesNA07029, NA18504, NA12155, NA18563, NA18860, NA07048, NA12872
Known GenesRBMY1A1, RBMY1B, RBMY1D, RBMY1E, TTTY13
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)nsv10026
Frequency
Sample Size31
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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