A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9166



Internal ID15534698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:111225410..111270267hg38UCSC Ensembl
Outerchr13:111877757..111922614hg19UCSC Ensembl
Outerchr13:110675758..110720615hg18UCSC Ensembl
Outerchr13:110675758..110720615hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3844858
hg1944858
hg1844858
hg1744858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1186
Supporting Variants
SamplesNA12156
Known GenesARHGEF7
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)nssv9166
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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