A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1928



Internal ID15194525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:20635647..20680091hg38UCSC Ensembl
Outerchr11:20657193..20701637hg19UCSC Ensembl
Outerchr11:20613769..20658213hg18UCSC Ensembl
Outerchr11:20613769..20658213hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3844445
hg1944445
hg1844445
hg1744445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7703
Supporting Variants
SamplesNA18555
Known GenesNELL1, SLC6A5
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)nssv1928
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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