A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518419



Internal ID15445712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:6547011..6547398hg38UCSC Ensembl
Innerchr18:6547010..6547397hg19UCSC Ensembl
Innerchr18:6537010..6537397hg18UCSC Ensembl
Innerchr18:6537010..6537397hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38388
hg19388
hg18388
hg17388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv185n21
Supporting Variantsnssv695854
Samples
Known GenesC18orf64
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518419
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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