A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2658



Internal ID15547221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:29136585..29181563hg38UCSC Ensembl
Outerchr2:29359451..29404429hg19UCSC Ensembl
Outerchr2:29212955..29257933hg18UCSC Ensembl
Outerchr2:29271102..29316080hg17UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg3844979
hg1944979
hg1844979
hg1744979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7476
SamplesNA12156
Known GenesCLIP4
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)nsv2658
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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