A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1874



Internal ID15194392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:141580550..141635364hg38UCSC Ensembl
OuterchrX:140668671..140723494hg19UCSC Ensembl
OuterchrX:140496337..140551160hg18UCSC Ensembl
OuterchrX:140394191..140449014hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3854815
hg1954824
hg1854824
hg1754824
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7462
Supporting Variants
SamplesNA18555
Known GenesSPANXA1, SPANXA2, SPANXA2-OT1
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)nssv1874
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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