A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10893



Internal ID15192795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:55591549..55702883hg38UCSC Ensembl
Outerchr11:55359025..55470359hg19UCSC Ensembl
Outerchr11:55115601..55226935hg18UCSC Ensembl
Outerchr11:55115601..55226935hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38111335
hg19111335
hg18111335
hg17111335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv323
Supporting Variants
SamplesNA15510
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
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)nssv10893
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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