A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv913



Internal ID15198119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:135145547..135186050hg38UCSC Ensembl
OuterchrX:134279474..134319978hg19UCSC Ensembl
OuterchrX:134107140..134147644hg18UCSC Ensembl
OuterchrX:134004994..134045498hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3840504
hg1940505
hg1840505
hg1740505
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7458
Supporting Variants
SamplesNA19240
Known GenesCXorf48
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)nssv913
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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