A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7743



Internal ID15552783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:39361003..39406343hg38UCSC Ensembl
Outerchr11:39382553..39427893hg19UCSC Ensembl
Outerchr11:39339129..39384469hg18UCSC Ensembl
Outerchr11:39339129..39384469hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3845341
hg1945341
hg1845341
hg1745341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6456
SamplesNA12156
Known Genes
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)nsv7743
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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