A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv361



Internal ID15201550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:65520835..65534840hg38UCSC Ensembl
Outerchr11:65288306..65302311hg19UCSC Ensembl
Outerchr11:65044882..65058887hg18UCSC Ensembl
Outerchr11:65044882..65058887hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3824576
hg1924576
hg1824576
hg1724576
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959
SamplesNA12878
Known GenesSCYL1
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)nsv361
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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