A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958



Internal ID15191999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:64326845..64359765hg38UCSC Ensembl
Outerchr11:64094317..64127237hg19UCSC Ensembl
Outerchr11:63850893..63883813hg18UCSC Ensembl
Outerchr11:63850893..63883813hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg386826
hg196826
hg186826
hg176826
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv358
Supporting Variants
SamplesNA12878
Known GenesCCDC88B, MIR7155, RPS6KA4
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)nssv3958
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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