A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7670



Internal ID15206017
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9941
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)nsv7670
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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