A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9812



Internal ID15193188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1882352..1916223hg38UCSC Ensembl
Outerchr11:1903582..1937453hg19UCSC Ensembl
Outerchr11:1860158..1894029hg18UCSC Ensembl
Outerchr11:1860158..1894029hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3833872
hg1933872
hg1833872
hg1733872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7643
Supporting Variants
SamplesNA18507
Known GenesLSP1
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)nssv9812
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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