A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3358



Internal ID15538086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:65878511..65891390hg38UCSC Ensembl
Outerchr5:65174339..65187218hg19UCSC Ensembl
Outerchr5:65210095..65222974hg18UCSC Ensembl
Outerchr5:65210095..65222974hg17UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg385186
hg195186
hg185186
hg175186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4864
Supporting Variants
SamplesNA12878
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)nssv3358
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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