A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468



Internal ID15551380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:6358344..6402978hg38UCSC Ensembl
Outerchr9:6358344..6402978hg19UCSC Ensembl
Outerchr9:6348344..6392978hg18UCSC Ensembl
Outerchr9:6348344..6392978hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg388068
hg198068
hg188068
hg178068
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10652, nssv5147
SamplesNA18956, NA19129
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)nsv6468
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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