A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4772



Internal ID15549515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:28512690..28529830hg38UCSC Ensembl
Outerchr5:28512797..28529937hg19UCSC Ensembl
Outerchr5:28548554..28565694hg18UCSC Ensembl
Outerchr5:28548554..28565694hg17UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3817141
hg1917141
hg1817141
hg1717141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8085
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)nsv4772
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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