A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7464



Internal ID15205790
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 StatusM
Merged Variants
Supporting Variantsnssv9255, nssv11229, nssv9783, nssv928, nssv5266, nssv927
SamplesNA18507, NA15510, NA18517, NA19240, NA19129
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)nsv7464
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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