A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26280



Internal ID15491036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:23144607..23164485hg38UCSC Ensembl
OuterchrY:23144276..23164977hg38UCSC Ensembl
InnerchrY:25290754..25310632hg19UCSC Ensembl
OuterchrY:25290423..25311124hg19UCSC Ensembl
InnerchrY:23700142..23720020hg18UCSC Ensembl
OuterchrY:23699811..23720512hg18UCSC Ensembl
InnerchrY:23628879..23648757hg17UCSC Ensembl
OuterchrY:23628548..23649249hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3820702
hg1920702
hg1820702
hg1720702
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)nssv26280
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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