A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5373



Internal ID15543061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93414197..93430059hg38UCSC Ensembl
Outerchr11:93147363..93163225hg19UCSC Ensembl
Outerchr11:92787011..92802873hg18UCSC Ensembl
Outerchr11:92787011..92802873hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3815863
hg1915863
hg1815863
hg1715863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv439
Supporting Variants
SamplesNA19129
Known GenesCCDC67
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)nssv5373
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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