A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11216



Internal ID15192677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49162987..49203711hg38UCSC Ensembl
OuterchrX:49017535..49060171hg19UCSC Ensembl
OuterchrX:48904479..48947115hg18UCSC Ensembl
OuterchrX:48773906..48816542hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3840725
hg1942637
hg1842637
hg1742637
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7442
Supporting Variants
SamplesNA15510
Known GenesMAGIX, PLP2, PRICKLE3, SYP
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)nssv11216
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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