A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580147



Internal ID16020870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54054505..54057172hg38UCSC Ensembl
Innerchr19:54557759..54560426hg19UCSC Ensembl
Innerchr19:59249571..59252238hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382668
hg192668
hg182668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6546n54
Supporting Variantsnssv901396
Samples
Known GenesVSTM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580147
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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