A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9941



Internal ID15540030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:9479348..9493203hg38UCSC Ensembl
Outerchr11:9500895..9514750hg19UCSC Ensembl
Outerchr11:9457471..9471326hg18UCSC Ensembl
Outerchr11:9457471..9471326hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3813856
hg1913856
hg1813856
hg1713856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7670
Supporting Variants
SamplesNA18507
Known GenesZNF143
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)nssv9941
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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