A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5334



Internal ID15196600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:960197..967940hg38UCSC Ensembl
Outerchr11:960197..967940hg19UCSC Ensembl
Outerchr11:950197..957940hg18UCSC Ensembl
Outerchr11:950197..957940hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg386869
hg196869
hg186869
hg176869
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7636
Supporting Variants
SamplesNA19129
Known GenesAP2A2
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)nssv5334
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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