A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11106



Internal ID15539602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:90140591..90156020hg38UCSC Ensembl
Outerchr5:89436408..89451837hg19UCSC Ensembl
Outerchr5:89472164..89487593hg18UCSC Ensembl
Outerchr5:89472164..89487593hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg389797
hg199797
hg189797
hg179797
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4912
Supporting Variants
SamplesNA15510
Known Genes
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)nssv11106
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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