A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25771



Internal ID15480548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:23232364..23264179hg38UCSC Ensembl
OuterchrY:23231872..23264510hg38UCSC Ensembl
InnerchrY:25378511..25410326hg19UCSC Ensembl
OuterchrY:25378019..25410657hg19UCSC Ensembl
InnerchrY:23787899..23819714hg18UCSC Ensembl
OuterchrY:23787407..23820045hg18UCSC Ensembl
InnerchrY:23716636..23748451hg17UCSC Ensembl
OuterchrY:23716144..23748782hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3832639
hg1932639
hg1832639
hg1732639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10034
Supporting Variants
SamplesNA07029
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)nssv25771
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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