A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1012



Internal ID15544796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:59260846..59292643hg38UCSC Ensembl
Outerchr11:59028319..59060116hg19UCSC Ensembl
Outerchr11:58784895..58816692hg18UCSC Ensembl
Outerchr11:58784895..58816692hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg389195
hg199195
hg189195
hg179195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv332
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)nssv1012
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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