A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10011



Internal ID15844974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:3629178..4669956hg38UCSC Ensembl
OuterchrY:3497219..4537997hg19UCSC Ensembl
OuterchrY:3557219..4597997hg18UCSC Ensembl
OuterchrY:3540580..4581358hg17UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg381040779
hg191040779
hg181040779
hg171040779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv27785, nssv26225, nssv25993
SamplesNA18504, NA07048, NA18853
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)nsv10011
Frequency
Sample Size31
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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