A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10799



Internal ID15541999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:4931002..4956452hg38UCSC Ensembl
Outerchr11:4952232..4977682hg19UCSC Ensembl
Outerchr11:4908808..4934258hg18UCSC Ensembl
Outerchr11:4908808..4934258hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3825451
hg1925451
hg1825451
hg1725451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7652
Supporting Variants
SamplesNA18956
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)nssv10799
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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