A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579874



Internal ID16020597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46119519..46123967hg38UCSC Ensembl
Innerchr19:46622776..46627224hg19UCSC Ensembl
Innerchr19:51314616..51319064hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg384449
hg194449
hg184449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6504n54
Supporting Variantsnssv899942, nssv899943
Samples
Known GenesIGFL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579874
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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