A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579522



Internal ID16020245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39895265..39899826hg38UCSC Ensembl
Innerchr19:40385905..40389923hg19UCSC Ensembl
Innerchr19:45077745..45081763hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg384562
hg194019
hg184019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899384
Samples
Known GenesFCGBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579522
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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