A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1028



Internal ID15545152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:92307624..92338498hg38UCSC Ensembl
Outerchr11:92040790..92071664hg19UCSC Ensembl
Outerchr11:91680438..91711312hg18UCSC Ensembl
Outerchr11:91680438..91711312hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3810102
hg1910102
hg1810102
hg1710102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv431
Supporting Variants
SamplesNA19240
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)nssv1028
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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