A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7742



Internal ID15552782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:38757341..38792059hg38UCSC Ensembl
Outerchr11:38778891..38813609hg19UCSC Ensembl
Outerchr11:38735467..38770185hg18UCSC Ensembl
Outerchr11:38735467..38770185hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg385016
hg195016
hg185016
hg175016
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3941
SamplesNA12878
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)nsv7742
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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