A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7692



Internal ID15552727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:17266058..17299821hg38UCSC Ensembl
Outerchr11:17287605..17321368hg19UCSC Ensembl
Outerchr11:17244181..17277944hg18UCSC Ensembl
Outerchr11:17244181..17277944hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg385669
hg195669
hg185669
hg175669
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8886
SamplesNA12156
Known GenesNUCB2
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)nsv7692
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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