A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10795



Internal ID15195317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3281072..3340945hg38UCSC Ensembl
Outerchr11:3302302..3362175hg19UCSC Ensembl
Outerchr11:3258878..3318751hg18UCSC Ensembl
Outerchr11:3258878..3318751hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3859874
hg1959874
hg1859874
hg1759874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7649
Supporting Variants
SamplesNA18956
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)nssv10795
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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