A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5274



Internal ID15196903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:154310039..154385078hg38UCSC Ensembl
OuterchrX:153538391..153613438hg19UCSC Ensembl
OuterchrX:153191585..153266632hg18UCSC Ensembl
OuterchrX:153059238..153134285hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3875040
hg1975048
hg1875048
hg1775048
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7468
Supporting Variants
SamplesNA19129
Known GenesEMD, FLNA, 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)nssv5274
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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