A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv398



Internal ID15548643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:77787954..77820182hg38UCSC Ensembl
Outerchr11:77499000..77531228hg19UCSC Ensembl
Outerchr11:77176648..77208876hg18UCSC Ensembl
Outerchr11:77176648..77208876hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg387277
hg197277
hg187277
hg177277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10830
SamplesNA18956
Known GenesRSF1
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)nsv398
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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