A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3805



Internal ID15201765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:47424312..47457614hg38UCSC Ensembl
Outerchr3:47465802..47499104hg19UCSC Ensembl
Outerchr3:47440806..47474108hg18UCSC Ensembl
Outerchr3:47440806..47474108hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg385984
hg195984
hg185984
hg175984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5962
SamplesNA19129
Known GenesSCAP
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)nsv3805
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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