A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4163



Internal ID15548845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:188956314..189001460hg38UCSC Ensembl
Outerchr3:188674103..188719249hg19UCSC Ensembl
Outerchr3:190156797..190201943hg18UCSC Ensembl
Outerchr3:190156805..190201951hg17UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3845147
hg1945147
hg1845147
hg1745147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4706
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)nsv4163
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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