A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10029



Internal ID15844992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:22165449..22187587hg38UCSC Ensembl
OuterchrY:24311596..24333734hg19UCSC Ensembl
OuterchrY:22720984..22743122hg18UCSC Ensembl
OuterchrY:22649721..22671859hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3822139
hg1922139
hg1822139
hg1722139
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26581, nssv27649, nssv25653, nssv23629, nssv27945, nssv26148, nssv28326
SamplesNA07029, NA18504, NA12155, NA18563, NA18860, NA07048, NA12872
Known GenesRBMY1F, RBMY1J
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)nsv10029
Frequency
Sample Size31
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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