A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3259



Internal ID15537987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:59945449..59980863hg38UCSC Ensembl
Outerchr4:60811167..60846581hg19UCSC Ensembl
Outerchr4:60493762..60529176hg18UCSC Ensembl
Outerchr4:60639933..60675347hg17UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg384322
hg194322
hg184322
hg174322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4355
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)nssv3259
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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