A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8916



Internal ID15188262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:59896327..59941631hg38UCSC Ensembl
Outerchr11:59663800..59709104hg19UCSC Ensembl
Outerchr11:59420376..59465680hg18UCSC Ensembl
Outerchr11:59420376..59465680hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3845305
hg1945305
hg1845305
hg1745305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv334
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)nssv8916
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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