A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5286



Internal ID15196815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:12966842..13119565hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg17152724
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7172
Supporting Variants
SamplesNA19129
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)nssv5286
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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