A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4686



Internal ID15543082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:144883131..144896615hg38UCSC Ensembl
Outerchr3:144601973..144615457hg19UCSC Ensembl
Outerchr3:146084663..146098147hg18UCSC Ensembl
Outerchr3:146084671..146098155hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg386333
hg196333
hg186333
hg176333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4044
Supporting Variants
SamplesNA19129
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)nssv4686
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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