A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511561



Internal ID15850986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23037020..23038073hg38UCSC Ensembl
Outerchr16:23034551..23039705hg38UCSC Ensembl
Innerchr16:23048341..23049394hg19UCSC Ensembl
Outerchr16:23045872..23051026hg19UCSC Ensembl
Innerchr16:22955842..22956895hg18UCSC Ensembl
Outerchr16:22953373..22958527hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg385155
hg195155
hg185155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626186
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)nsv511561
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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