A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511605



Internal ID15851030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:41284939..41288040hg38UCSC Ensembl
Outerchr18:41282183..41293868hg38UCSC Ensembl
Innerchr18:38864903..38868004hg19UCSC Ensembl
Outerchr18:38862147..38873832hg19UCSC Ensembl
Innerchr18:37118901..37122002hg18UCSC Ensembl
Outerchr18:37116145..37127830hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3811686
hg1911686
hg1811686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626235
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511605
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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