A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8978



Internal ID15534886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:128807180..128826472hg38UCSC Ensembl
Outerchr11:128677075..128696367hg19UCSC Ensembl
Outerchr11:128182285..128201577hg18UCSC Ensembl
Outerchr11:128182285..128201577hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3819293
hg1919293
hg1819293
hg1719293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545
Supporting Variants
SamplesNA12156
Known GenesFLI1
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)nssv8978
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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