A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1011



Internal ID15544806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:57984177..58005746hg38UCSC Ensembl
Outerchr11:57751649..57773218hg19UCSC Ensembl
Outerchr11:57508225..57529794hg18UCSC Ensembl
Outerchr11:57508225..57529794hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3821570
hg1921570
hg1821570
hg1721570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv328
Supporting Variants
SamplesNA19240
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)nssv1011
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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