A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6468



Internal ID15537396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:68543602..68572674hg38UCSC Ensembl
Outerchr11:68311070..68340142hg19UCSC Ensembl
Outerchr11:68067646..68096718hg18UCSC Ensembl
Outerchr11:68067646..68096718hg17UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3829073
hg1929073
hg1829073
hg1729073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv372
Supporting Variants
SamplesNA12156
Known GenesPPP6R3
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)nssv6468
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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