A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578455



Internal ID16019178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4851838..4878596hg38UCSC Ensembl
Innerchr19:4851850..4878608hg19UCSC Ensembl
Innerchr19:4802850..4829608hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3826759
hg1926759
hg1826759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv892937
Samples
Known GenesPLIN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578455
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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