A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5266



Internal ID15196966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:148539516..148605471hg18UCSC Ensembl
OuterchrX:148437370..148503325hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg1865956
hg1765956
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7464
Supporting Variants
SamplesNA19129
Known GenesMAGEA11
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv5266
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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