A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7683



Internal ID15552717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:12613009..12647438hg38UCSC Ensembl
Outerchr11:12634556..12668985hg19UCSC Ensembl
Outerchr11:12591132..12625561hg18UCSC Ensembl
Outerchr11:12591132..12625561hg17UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg385318
hg195318
hg185318
hg175318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3928
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)nsv7683
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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