A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579239



Internal ID16366648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28699611..28745959hg38UCSC Ensembl
Innerchr19:29190518..29236866hg19UCSC Ensembl
Innerchr19:33882358..33928706hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3846349
hg1946349
hg1846349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv897469
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579239
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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