A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv369



Internal ID15201638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:67801134..67815456hg38UCSC Ensembl
Outerchr11:67568605..67582927hg19UCSC Ensembl
Outerchr11:67325181..67339503hg18UCSC Ensembl
Outerchr11:67325181..67339503hg17UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg388336
hg198336
hg188336
hg178336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10826
SamplesNA18956
Known GenesFAM86C2P
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)nsv369
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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