A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10039



Internal ID15845002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:26120101..26121315hg38UCSC Ensembl
OuterchrY:28266248..28267462hg19UCSC Ensembl
OuterchrY:26675636..26676850hg18UCSC Ensembl
OuterchrY:26604373..26605587hg17UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg381215
hg191215
hg181215
hg171215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26271
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)nsv10039
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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