A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10032



Internal ID15844995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:22645671..22646886hg38UCSC Ensembl
OuterchrY:24791818..24793033hg19UCSC Ensembl
OuterchrY:23201206..23202421hg18UCSC Ensembl
OuterchrY:23129943..23131158hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg381216
hg191216
hg181216
hg171216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26235
SamplesNA07048
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)nsv10032
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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