A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419



Internal ID15544290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:67283041..67308057hg38UCSC Ensembl
Outerchr18:64950278..64975294hg19UCSC Ensembl
Outerchr18:63101258..63126274hg18UCSC Ensembl
Outerchr18:63101258..63126274hg17UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3825017
hg1925017
hg1825017
hg1725017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2341
Supporting Variants
SamplesNA19240
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)nssv1419
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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