A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11093



Internal ID15539615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:155946309..155970334hg38UCSC Ensembl
Outerchr4:156867461..156891486hg19UCSC Ensembl
Outerchr4:157086911..157110936hg18UCSC Ensembl
Outerchr4:157225066..157249091hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3814192
hg1914192
hg1814192
hg1714192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4564
Supporting Variants
SamplesNA15510
Known GenesCTSO
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)nssv11093
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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