A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3837



Internal ID15548486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:58017147..58045161hg38UCSC Ensembl
Outerchr3:58002874..58030888hg19UCSC Ensembl
Outerchr3:57977914..58005928hg18UCSC Ensembl
Outerchr3:57977914..58005928hg17UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg388513
hg198513
hg188513
hg178513
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7011
SamplesNA12156
Known GenesFLNB
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)nsv3837
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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