A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4023



Internal ID15202005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:136053356..136097793hg38UCSC Ensembl
Outerchr3:135772198..135816635hg19UCSC Ensembl
Outerchr3:137254888..137299325hg18UCSC Ensembl
Outerchr3:137254896..137299333hg17UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3844438
hg1944438
hg1844438
hg1744438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4667
SamplesNA19129
Known GenesPPP2R3A
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)nsv4023
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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