A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7718



Internal ID15552755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:26110104..26138911hg38UCSC Ensembl
Outerchr11:26131651..26160458hg19UCSC Ensembl
Outerchr11:26088227..26117034hg18UCSC Ensembl
Outerchr11:26088227..26117034hg17UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg3810698
hg1910698
hg1810698
hg1710698
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10810
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)nsv7718
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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