A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579513



Internal ID16366922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39877882..39895265hg38UCSC Ensembl
Innerchr19:40368522..40385905hg19UCSC Ensembl
Innerchr19:45060362..45077745hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3817384
hg1917384
hg1817384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6440n54
Supporting Variantsnssv899264
Samples
Known GenesFCGBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579513
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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