A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10016



Internal ID15844979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:9893780..9909819hg38UCSC Ensembl
OuterchrY:9731389..9747428hg19UCSC Ensembl
OuterchrY:10341389..10357428hg18UCSC Ensembl
OuterchrY:10324750..10340789hg17UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3816040
hg1916040
hg1816040
hg1716040
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26244, nssv23966, nssv27850, nssv26820, nssv27216
SamplesNA18504, NA18572, NA18853, NA19144, NA19173
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)nsv10016
Frequency
Sample Size31
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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