A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3952



Internal ID15538679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:56695366..56703796hg38UCSC Ensembl
Outerchr11:56462842..56471272hg19UCSC Ensembl
Outerchr11:56219418..56227848hg18UCSC Ensembl
Outerchr11:56219418..56227848hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3810886
hg1910886
hg1810886
hg1710886
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv325
Supporting Variants
SamplesNA12878
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)nssv3952
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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