A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6443



Internal ID15537421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:4929729..4976539hg38UCSC Ensembl
Outerchr11:4950959..4997769hg19UCSC Ensembl
Outerchr11:4907535..4954345hg18UCSC Ensembl
Outerchr11:4907535..4954345hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3846811
hg1946811
hg1846811
hg1746811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7652
Supporting Variants
SamplesNA12156
Known GenesOR51A2, OR51A4
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)nssv6443
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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