A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579880



Internal ID16020603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46119519..46125856hg38UCSC Ensembl
Innerchr19:46622776..46629113hg19UCSC Ensembl
Innerchr19:51314616..51320953hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg386338
hg196338
hg186338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6504n54
Supporting Variantsnssv899962, nssv899963
Samples
Known GenesIGFL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579880
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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