A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861



Internal ID15198273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:46810806..46871811hg19UCSC Ensembl
OuterchrX:46695750..46756755hg18UCSC Ensembl
OuterchrX:46567060..46628065hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg1961006
hg1861006
hg1761006
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7440
Supporting Variants
SamplesNA19240
Known GenesJADE3
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)nssv861
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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