A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1926



Internal ID15541209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:4925015..4958926hg38UCSC Ensembl
Outerchr11:4946245..4980156hg19UCSC Ensembl
Outerchr11:4902821..4936732hg18UCSC Ensembl
Outerchr11:4902821..4936732hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3833912
hg1933912
hg1833912
hg1733912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7652
Supporting Variants
SamplesNA18555
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)nssv1926
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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