A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4583



Internal ID15549307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:161306244..161350966hg38UCSC Ensembl
Outerchr4:162227396..162272118hg19UCSC Ensembl
Outerchr4:162446846..162491568hg18UCSC Ensembl
Outerchr4:162585001..162629723hg17UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3844723
hg1944723
hg1844723
hg1744723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8021
SamplesNA12156
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)nsv4583
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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