A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4816



Internal ID15543105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:3890782..3899259hg38UCSC Ensembl
Outerchr5:3890896..3899373hg19UCSC Ensembl
Outerchr5:3943896..3952373hg18UCSC Ensembl
Outerchr5:3943896..3952373hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg386310
hg196310
hg186310
hg176310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4686
Supporting Variants
SamplesNA19129
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)nssv4816
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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