A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579521



Internal ID16366930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39894900..39895214hg38UCSC Ensembl
Innerchr19:40385540..40385854hg19UCSC Ensembl
Innerchr19:45077380..45077694hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38315
hg19315
hg18315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899383
Samples
Known GenesFCGBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579521
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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