A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6380



Internal ID15190798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:134856413..134985866hg19UCSC Ensembl
OuterchrX:134684079..134813532hg18UCSC Ensembl
OuterchrX:134581933..134711386hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg19129454
hg18129454
hg17129454
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7460
Supporting Variants
SamplesNA12156
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)nssv6380
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer