A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26262



Internal ID15491181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:23141096..23143068hg38UCSC Ensembl
OuterchrY:23140213..23143307hg38UCSC Ensembl
InnerchrY:25287243..25289215hg19UCSC Ensembl
OuterchrY:25286360..25289454hg19UCSC Ensembl
InnerchrY:23696631..23698603hg18UCSC Ensembl
OuterchrY:23695748..23698842hg18UCSC Ensembl
InnerchrY:23625368..23627340hg17UCSC Ensembl
OuterchrY:23624485..23627579hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg383095
hg193095
hg183095
hg173095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10034
Supporting Variants
SamplesNA18853
Known GenesDAZ1, 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)nssv26262
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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