A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv865



Internal ID15198290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49162987..49198621hg38UCSC Ensembl
OuterchrX:49017409..49055080hg19UCSC Ensembl
OuterchrX:48904353..48942024hg18UCSC Ensembl
OuterchrX:48773780..48811451hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3835635
hg1937672
hg1837672
hg1737672
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7442
Supporting Variants
SamplesNA19240
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)nssv865
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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