A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511617



Internal ID15504356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:32720222..32720801hg38UCSC Ensembl
Outerchr19:32719341..32730420hg38UCSC Ensembl
Innerchr19:33211128..33211707hg19UCSC Ensembl
Outerchr19:33210247..33221326hg19UCSC Ensembl
Innerchr19:37902968..37903547hg18UCSC Ensembl
Outerchr19:37902087..37913166hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3811080
hg1911080
hg1811080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626248
Samples1
Known GenesTDRD12
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511617
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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