A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3322



Internal ID15538050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:4884083..4919010hg38UCSC Ensembl
Outerchr5:4884196..4919123hg19UCSC Ensembl
Outerchr5:4937196..4972123hg18UCSC Ensembl
Outerchr5:4937196..4972123hg17UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg384818
hg194818
hg184818
hg174818
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4689
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)nssv3322
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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