A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10839



Internal ID15541959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:110493336..110507965hg38UCSC Ensembl
Outerchr11:110364060..110378689hg19UCSC Ensembl
Outerchr11:109869270..109883899hg18UCSC Ensembl
Outerchr11:109869270..109883899hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg386389
hg196389
hg186389
hg176389
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv485
Supporting Variants
SamplesNA18956
Known Genes
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)nssv10839
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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