A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10018



Internal ID15498295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10177992..10193662hg38UCSC Ensembl
OuterchrY:10015601..10031271hg19UCSC Ensembl
OuterchrY:10625601..10641271hg18UCSC Ensembl
OuterchrY:10608962..10624632hg17UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3815671
hg1915671
hg1815671
hg1715671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv27857
SamplesNA18504
Known Genes
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)nsv10018
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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