A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9255



Internal ID15540206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:149560428..149958297hg38UCSC Ensembl
OuterchrX:148449878..148877173hg18UCSC Ensembl
OuterchrX:148347732..148797083hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38397870
hg18427296
hg17449352
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7464
Supporting Variants
SamplesNA18517
Known GenesCXorf40B, HSFX1, HSFX2, LINC00894, MAGEA11, MAGEA8, MAGEA8-AS1, MAGEA9, MAGEA9B, TMEM185A
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)nssv9255
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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