A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11231



Internal ID15192662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:154328000..154367048hg38UCSC Ensembl
OuterchrX:153556346..153595416hg19UCSC Ensembl
OuterchrX:153209540..153248610hg18UCSC Ensembl
OuterchrX:153077193..153116263hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3839049
hg1939071
hg1839071
hg1739071
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7468
Supporting Variants
SamplesNA15510
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)nssv11231
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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