A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10034



Internal ID15844997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:22728182..23526051hg38UCSC Ensembl
OuterchrY:24874329..25672198hg19UCSC Ensembl
OuterchrY:23283717..24081586hg18UCSC Ensembl
OuterchrY:23212454..24010323hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38797870
hg19797870
hg18797870
hg17797870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25771, nssv26622, nssv26280, nssv26842, nssv28362, nssv27681, nssv27969, nssv26609, nssv27673, nssv26831, nssv25749, nssv26512, nssv27236, nssv28366, nssv24050, nssv24023, nssv27226, nssv26262, nssv26297, nssv28364, nssv26635, nssv26314, nssv26526
SamplesNA07029, NA18504, NA12155, NA18563, NA18860, NA19007, NA18572, NA18853, NA19144, NA19173
Known GenesBPY2, BPY2B, BPY2C, DAZ1, DAZ2, DAZ3, DAZ4, TTTY17A, TTTY17B, TTTY17C, TTTY4, TTTY4B, TTTY4C
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)nsv10034
Frequency
Sample Size31
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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