A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5097



Internal ID15203186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:160371035..160413932hg38UCSC Ensembl
Outerchr5:159798042..159840939hg19UCSC Ensembl
Outerchr5:159730620..159773517hg18UCSC Ensembl
Outerchr5:159730620..159773517hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3842898
hg1942898
hg1842898
hg1742898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8179
SamplesNA12156
Known GenesC5orf54, SLU7
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)nsv5097
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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