A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5111



Internal ID15549888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:166408288..166439252hg38UCSC Ensembl
Outerchr5:165835293..165866257hg19UCSC Ensembl
Outerchr5:165767871..165798835hg18UCSC Ensembl
Outerchr5:165767871..165798835hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3830965
hg1930965
hg1830965
hg1730965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9417
SamplesNA18517
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)nsv5111
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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