A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580142



Internal ID16020865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54054016..54056773hg38UCSC Ensembl
Innerchr19:54557270..54560027hg19UCSC Ensembl
Innerchr19:59249082..59251839hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382758
hg192758
hg182758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6546n54
Supporting Variantsnssv901366
Samples
Known GenesVSTM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580142
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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