A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26923



Internal ID15842590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:57724292..57725332hg38UCSC Ensembl
OuterchrX:57715300..57731510hg38UCSC Ensembl
InnerchrX:57750725..57751765hg19UCSC Ensembl
OuterchrX:57741733..57757943hg19UCSC Ensembl
InnerchrX:57767450..57768490hg18UCSC Ensembl
OuterchrX:57758458..57774668hg18UCSC Ensembl
InnerchrX:57633746..57634786hg17UCSC Ensembl
OuterchrX:57624754..57640964hg17UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg3816211
hg1916211
hg1816211
hg1716211
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9948
Supporting Variants
SamplesNA19144
Known Genes
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)nssv26923
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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