A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5335



Internal ID15196591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1016041..1017988hg38UCSC Ensembl
Outerchr11:1016041..1017988hg19UCSC Ensembl
Outerchr11:1006041..1007988hg18UCSC Ensembl
Outerchr11:1006041..1007988hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg388907
hg198907
hg188907
hg178907
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7637
Supporting Variants
SamplesNA19129
Known GenesMUC6
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)nssv5335
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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