A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579908



Internal ID16020631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:49645135..49663393hg38UCSC Ensembl
Innerchr19:50148392..50166650hg19UCSC Ensembl
Innerchr19:54840204..54858462hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3818259
hg1918259
hg1818259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899991
Samples
Known GenesIRF3, SCAF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579908
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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