A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511579



Internal ID15851004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11590156..11590572hg38UCSC Ensembl
Outerchr16:11587866..11595035hg38UCSC Ensembl
Innerchr16:11684012..11684428hg19UCSC Ensembl
Outerchr16:11681722..11688891hg19UCSC Ensembl
Innerchr16:11591513..11591929hg18UCSC Ensembl
Outerchr16:11589223..11596392hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg387170
hg197170
hg187170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626206
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)nsv511579
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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