A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3879



Internal ID15548532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:73657607..73694272hg38UCSC Ensembl
Outerchr3:73706758..73743423hg19UCSC Ensembl
Outerchr3:73789448..73826113hg18UCSC Ensembl
Outerchr3:73789448..73826113hg17UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3836666
hg1936666
hg1836666
hg1736666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7828
SamplesNA12156
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)nsv3879
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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