A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11122



Internal ID15192771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:26697138..26811271hg19UCSC Ensembl
Outerchr6:26805117..26919250hg18UCSC Ensembl
Outerchr6:26805117..26919250hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg19114134
hg18114134
hg17114134
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7378
Supporting Variants
SamplesNA15510
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)nssv11122
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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