A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3680



Internal ID15548314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:3853197..3886546hg38UCSC Ensembl
Outerchr3:3894881..3928230hg19UCSC Ensembl
Outerchr3:3869881..3903230hg18UCSC Ensembl
Outerchr3:3869881..3903230hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg386082
hg196082
hg186082
hg176082
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7766
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)nsv3680
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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