A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7458



Internal ID15205783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:135145248..135269268hg38UCSC Ensembl
OuterchrX:134279175..134403214hg19UCSC Ensembl
OuterchrX:134106841..134230880hg18UCSC Ensembl
OuterchrX:134004695..134128734hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38124021
hg19124040
hg18124040
hg17124040
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6376, nssv6377, nssv913, nssv914, nssv5260
SamplesNA12156, NA19240, NA19129
Known GenesCXorf48
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)nsv7458
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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