A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1009



Internal ID15544821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:56693595..56705212hg38UCSC Ensembl
Outerchr11:56461071..56472688hg19UCSC Ensembl
Outerchr11:56217647..56229264hg18UCSC Ensembl
Outerchr11:56217647..56229264hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3810942
hg1910942
hg1810942
hg1710942
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv325
Supporting Variants
SamplesNA19240
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)nssv1009
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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