A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv356



Internal ID15548181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:64101375..64145657hg38UCSC Ensembl
Outerchr11:63868847..63913129hg19UCSC Ensembl
Outerchr11:63625423..63669705hg18UCSC Ensembl
Outerchr11:63625423..63669705hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3844283
hg1944283
hg1844283
hg1744283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1943
SamplesNA18555
Known GenesFLRT1, MACROD1
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)nsv356
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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