A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7687



Internal ID15552721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:16699259..16732490hg38UCSC Ensembl
Outerchr11:16720806..16754037hg19UCSC Ensembl
Outerchr11:16677382..16710613hg18UCSC Ensembl
Outerchr11:16677382..16710613hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg386499
hg196499
hg186499
hg176499
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3929
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)nsv7687
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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