A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7455



Internal ID15552466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:106239923..106327965hg38UCSC Ensembl
OuterchrX:105483139..105571192hg19UCSC Ensembl
OuterchrX:105369795..105457848hg18UCSC Ensembl
OuterchrX:105289284..105377337hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3888043
hg1988054
hg1888054
hg1788054
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10724, nssv899, nssv9487, nssv900
SamplesNA18956, NA18517, NA19240
Known Genes
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)nsv7455
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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