A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8974



Internal ID15188204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:125462800..125488621hg38UCSC Ensembl
Outerchr11:125332696..125358517hg19UCSC Ensembl
Outerchr11:124837906..124863727hg18UCSC Ensembl
Outerchr11:124837906..124863727hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3825822
hg1925822
hg1825822
hg1725822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv532
Supporting Variants
SamplesNA12156
Known GenesFEZ1
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)nssv8974
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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