A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10701



Internal ID15195411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:46812278..46867180hg19UCSC Ensembl
OuterchrX:46697222..46752124hg18UCSC Ensembl
OuterchrX:46568532..46623434hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg1954903
hg1854903
hg1754903
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7440
Supporting Variants
SamplesNA18956
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)nssv10701
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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