A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7644



Internal ID15552674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1931813..1944658hg38UCSC Ensembl
Outerchr11:1953043..1965888hg19UCSC Ensembl
Outerchr11:1909619..1922464hg18UCSC Ensembl
Outerchr11:1909619..1922464hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3823641
hg1923641
hg1823641
hg1723641
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3918, nssv10885, nssv5342, nssv985
SamplesNA12878, NA15510, NA19240, NA19129
Known GenesTNNT3
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)nsv7644
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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