A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26526



Internal ID15494856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:23232364..23257162hg38UCSC Ensembl
OuterchrY:23231872..23257829hg38UCSC Ensembl
InnerchrY:25378511..25403309hg19UCSC Ensembl
OuterchrY:25378019..25403976hg19UCSC Ensembl
InnerchrY:23787899..23812697hg18UCSC Ensembl
OuterchrY:23787407..23813364hg18UCSC Ensembl
InnerchrY:23716636..23741434hg17UCSC Ensembl
OuterchrY:23716144..23742101hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3825958
hg1925958
hg1825958
hg1725958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10034
Supporting Variants
SamplesNA19007
Known GenesDAZ2, DAZ3, DAZ4
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)nssv26526
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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