A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579518



Internal ID16020241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39894797..39896716hg38UCSC Ensembl
Innerchr19:40385437..40387356hg19UCSC Ensembl
Innerchr19:45077277..45079196hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381920
hg191920
hg181920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899271
Samples
Known GenesFCGBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579518
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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