A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9258



Internal ID15193523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:154310628..154378192hg38UCSC Ensembl
OuterchrX:153538979..153606552hg19UCSC Ensembl
OuterchrX:153192173..153259746hg18UCSC Ensembl
OuterchrX:153059826..153127399hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3867565
hg1967574
hg1867574
hg1767574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7468
Supporting Variants
SamplesNA18517
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)nssv9258
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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