A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1036



Internal ID15545106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:107353856..107384996hg38UCSC Ensembl
Outerchr11:107224582..107255722hg19UCSC Ensembl
Outerchr11:106729792..106760932hg18UCSC Ensembl
Outerchr11:106729792..106760932hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3831141
hg1931141
hg1831141
hg1731141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv475
Supporting Variants
SamplesNA19240
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)nssv1036
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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