A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578164



Internal ID16018887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:647039..675513hg38UCSC Ensembl
Innerchr19:647039..675513hg19UCSC Ensembl
Innerchr19:598039..626513hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3828475
hg1928475
hg1828475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891234
Samples
Known GenesRNF126
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578164
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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