A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7462



Internal ID15205788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:140964264..141635364hg38UCSC Ensembl
OuterchrX:140046429..140723494hg19UCSC Ensembl
OuterchrX:139874095..140551160hg18UCSC Ensembl
OuterchrX:139771949..140449014hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38671101
hg19677066
hg18677066
hg17677066
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5264, nssv1872, nssv1874
SamplesNA18555, NA19129
Known GenesLDOC1, SPANXA1, SPANXA2, SPANXA2-OT1, SPANXB1, SPANXB2, SPANXC, SPANXF1
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)nsv7462
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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