A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5261



Internal ID15197003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:134856051..134949308hg19UCSC Ensembl
OuterchrX:134683717..134776974hg18UCSC Ensembl
OuterchrX:134581571..134674828hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg1993258
hg1893258
hg1793258
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7460
Supporting Variants
SamplesNA19129
Known GenesCT45A1, CT45A2, CT45A3, CT45A4, CT45A5
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)nssv5261
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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