A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9747



Internal ID15539845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:48178035..48229828hg19UCSC Ensembl
Outerchr8:48340588..48392381hg18UCSC Ensembl
Outerchr8:48340588..48392381hg17UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg1951794
hg1851794
hg1751794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7416
Supporting Variants
SamplesNA18507
Known GenesSPIDR
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)nssv9747
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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