A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2360



Internal ID15546923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:75060637..75105952hg38UCSC Ensembl
Outerchr18:72772593..72817908hg19UCSC Ensembl
Outerchr18:70901581..70946896hg18UCSC Ensembl
Outerchr18:70901581..70946896hg17UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3845316
hg1945316
hg1845316
hg1745316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5711
SamplesNA19129
Known GenesZNF407
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)nsv2360
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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