A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9270



Internal ID15540221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:56693303..56706110hg38UCSC Ensembl
Outerchr11:56460779..56473586hg19UCSC Ensembl
Outerchr11:56217355..56230162hg18UCSC Ensembl
Outerchr11:56217355..56230162hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3814286
hg1914286
hg1814286
hg1714286
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv325
Supporting Variants
SamplesNA18517
Known GenesOR9G1, OR9G9
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)nssv9270
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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