A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9275



Internal ID15540226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:107341074..107381994hg38UCSC Ensembl
Outerchr11:107211800..107252720hg19UCSC Ensembl
Outerchr11:106717010..106757930hg18UCSC Ensembl
Outerchr11:106717010..106757930hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3840921
hg1940921
hg1840921
hg1740921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv475
Supporting Variants
SamplesNA18517
Known GenesCWF19L2
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)nssv9275
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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