A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9785



Internal ID15193155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:154317289..154378577hg38UCSC Ensembl
OuterchrX:153545637..153606937hg19UCSC Ensembl
OuterchrX:153198831..153260131hg18UCSC Ensembl
OuterchrX:153066484..153127784hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3861289
hg1961301
hg1861301
hg1761301
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7468
Supporting Variants
SamplesNA18507
Known GenesFLNA, TKTL1
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)nssv9785
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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