A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579863



Internal ID16020586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44807062..44819194hg38UCSC Ensembl
Innerchr19:45310319..45322451hg19UCSC Ensembl
Innerchr19:50002159..50014291hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3812133
hg1912133
hg1812133
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899928
Samples
Known GenesBCAM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579863
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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