A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579565



Internal ID16366974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40850594..40873243hg38UCSC Ensembl
Innerchr19:41356499..41379148hg19UCSC Ensembl
Innerchr19:46048339..46070988hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3822650
hg1922650
hg1822650
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6448n54
Supporting Variantsnssv899468, nssv899467
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579565
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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