A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3779



Internal ID15191192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:46769024..46830526hg19UCSC Ensembl
OuterchrX:46653968..46715470hg18UCSC Ensembl
OuterchrX:46525278..46586780hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg1961503
hg1861503
hg1761503
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7440
Supporting Variants
SamplesNA12878
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)nssv3779
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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