A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9128



Internal ID15534736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:54892411..54937157hg38UCSC Ensembl
Outerchr13:55466546..55511292hg19UCSC Ensembl
Outerchr13:54364547..54409293hg18UCSC Ensembl
Outerchr13:54364547..54409293hg17UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3844747
hg1944747
hg1844747
hg1744747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051
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)nssv9128
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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