A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9113



Internal ID15188065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:36729306..36774100hg38UCSC Ensembl
Outerchr13:37303443..37348237hg19UCSC Ensembl
Outerchr13:36201443..36246237hg18UCSC Ensembl
Outerchr13:36201443..36246237hg17UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3844795
hg1944795
hg1844795
hg1744795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005
Supporting Variants
SamplesNA12156
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)nssv9113
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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