A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4013



Internal ID15548680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:132479631..132524724hg38UCSC Ensembl
Outerchr3:132198475..132243568hg19UCSC Ensembl
Outerchr3:133681165..133726258hg18UCSC Ensembl
Outerchr3:133681173..133726266hg17UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3845094
hg1945094
hg1845094
hg1745094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7868
SamplesNA12156
Known GenesDNAJC13
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)nsv4013
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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