A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27555



Internal ID15830739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141905801..141906677hg38UCSC Ensembl
OuterchrX:141905268..141906980hg38UCSC Ensembl
InnerchrX:140993587..140994463hg19UCSC Ensembl
OuterchrX:140993054..140994766hg19UCSC Ensembl
InnerchrX:140821253..140822129hg18UCSC Ensembl
OuterchrX:140820720..140822432hg18UCSC Ensembl
InnerchrX:140719107..140719983hg17UCSC Ensembl
OuterchrX:140718574..140720286hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg381713
hg191713
hg181713
hg171713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9985
Supporting Variants
SamplesNA12155
Known GenesMAGEC1
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)nssv27555
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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