A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5260



Internal ID15197013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:135145248..135265946hg38UCSC Ensembl
OuterchrX:134279175..134399892hg19UCSC Ensembl
OuterchrX:134106841..134227558hg18UCSC Ensembl
OuterchrX:134004695..134125412hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38120699
hg19120718
hg18120718
hg17120718
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7458
Supporting Variants
SamplesNA19129
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)nssv5260
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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