A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7421



Internal ID15189757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:79743016..79773672hg38UCSC Ensembl
Outerchr18:77503016..77533672hg19UCSC Ensembl
Outerchr18:75604004..75634660hg18UCSC Ensembl
Outerchr18:75604004..75634660hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3830657
hg1930657
hg1830657
hg1730657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2382
Supporting Variants
SamplesNA12156
Known GenesCTDP1
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)nssv7421
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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