A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv915



Internal ID15198133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:135720375..135903654hg38UCSC Ensembl
OuterchrX:134862556..134985813hg19UCSC Ensembl
OuterchrX:134690222..134813479hg18UCSC Ensembl
OuterchrX:134588076..134711333hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38183280
hg19123258
hg18123258
hg17123258
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7460
Supporting Variants
SamplesNA19240
Known GenesCT45A2, CT45A3, CT45A4, CT45A5, CT45A6, SAGE1
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)nssv915
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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