A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7460



Internal ID15205786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:135703429..135914069hg38UCSC Ensembl
OuterchrX:134837144..134996228hg19UCSC Ensembl
OuterchrX:134664810..134823894hg18UCSC Ensembl
OuterchrX:134562664..134721748hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38210641
hg19159085
hg18159085
hg17159085
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6379, nssv915, nssv6380, nssv5261, nssv5262, nssv1871
SamplesNA12156, NA18555, NA19240, NA19129
Known GenesCT45A1, CT45A2, 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)nsv7460
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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