A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579876



Internal ID16020599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46119519..46124505hg38UCSC Ensembl
Innerchr19:46622776..46627762hg19UCSC Ensembl
Innerchr19:51314616..51319602hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg384987
hg194987
hg184987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6504n54
Supporting Variantsnssv899946, nssv899945
Samples
Known GenesIGFL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579876
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer