A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10791



Internal ID15195321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1536076..1546026hg38UCSC Ensembl
Outerchr11:1557306..1567256hg19UCSC Ensembl
Outerchr11:1513882..1523832hg18UCSC Ensembl
Outerchr11:1513882..1523832hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg387326
hg197326
hg187326
hg177326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7640
Supporting Variants
SamplesNA18956
Known GenesMOB2
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)nssv10791
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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