A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9274



Internal ID15540225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:101663376..101709185hg38UCSC Ensembl
Outerchr11:101534107..101579916hg19UCSC Ensembl
Outerchr11:101039317..101085126hg18UCSC Ensembl
Outerchr11:101039317..101085126hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3845810
hg1945810
hg1845810
hg1745810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv461
Supporting Variants
SamplesNA18517
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)nssv9274
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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