A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26635



Internal ID15489322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:23030364..23495481hg38UCSC Ensembl
OuterchrY:23030094..23495932hg38UCSC Ensembl
InnerchrY:25176511..25641628hg19UCSC Ensembl
OuterchrY:25176241..25642079hg19UCSC Ensembl
InnerchrY:23585899..24051016hg18UCSC Ensembl
OuterchrY:23585629..24051467hg18UCSC Ensembl
InnerchrY:23514636..23979753hg17UCSC Ensembl
OuterchrY:23514366..23980204hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38465839
hg19465839
hg18465839
hg17465839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10034
Supporting Variants
SamplesNA18563
Known GenesDAZ1, DAZ2, 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)nssv26635
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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