A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3411



Internal ID15191453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:179918100..179952089hg38UCSC Ensembl
Outerchr5:179345100..179379089hg19UCSC Ensembl
Outerchr5:179277706..179311695hg18UCSC Ensembl
Outerchr5:179277706..179311695hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg385758
hg195758
hg185758
hg175758
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5161
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)nssv3411
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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