A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8930



Internal ID15534934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:70367740..70392262hg38UCSC Ensembl
Outerchr11:70213846..70238368hg19UCSC Ensembl
Outerchr11:69891494..69916016hg18UCSC Ensembl
Outerchr11:69891494..69916016hg17UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg386968
hg196968
hg186968
hg176968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv379
Supporting Variants
SamplesNA12156
Known GenesPPFIA1
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)nssv8930
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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