A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv334



Internal ID15201253
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 StatusM
Merged Variants
Supporting Variantsnssv8916
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)nsv334
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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