A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511623



Internal ID15851048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50903716..50904679hg38UCSC Ensembl
Outerchr19:50897519..50905586hg38UCSC Ensembl
Innerchr19:51406972..51407935hg19UCSC Ensembl
Outerchr19:51400775..51408842hg19UCSC Ensembl
Innerchr19:56098784..56099747hg18UCSC Ensembl
Outerchr19:56092587..56100654hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg388068
hg198068
hg188068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626256
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)nsv511623
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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