A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10827



Internal ID15195285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:68880721..68894879hg38UCSC Ensembl
Outerchr11:68648189..68662347hg19UCSC Ensembl
Outerchr11:68404765..68418923hg18UCSC Ensembl
Outerchr11:68404765..68418923hg17UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg386499
hg196499
hg186499
hg176499
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv374
Supporting Variants
SamplesNA18956
Known GenesMRPL21
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)nssv10827
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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