A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579877



Internal ID16020600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46119519..46124823hg38UCSC Ensembl
Innerchr19:46622776..46628080hg19UCSC Ensembl
Innerchr19:51314616..51319920hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg385305
hg195305
hg185305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6504n54
Supporting Variantsnssv899947
Samples
Known GenesIGFL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579877
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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