A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5074



Internal ID15203161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:152631131..152676219hg38UCSC Ensembl
Outerchr5:152010691..152055779hg19UCSC Ensembl
Outerchr5:151990884..152035972hg18UCSC Ensembl
Outerchr5:151990884..152035972hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3845089
hg1945089
hg1845089
hg1745089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8169
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)nsv5074
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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