A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578304



Internal ID16019027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1566507..1567450hg38UCSC Ensembl
Innerchr19:1566506..1567449hg19UCSC Ensembl
Innerchr19:1517506..1518449hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38944
hg19944
hg18944
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6204n54
Supporting Variantsnssv891824, nssv891826, nssv891825
Samples
Known GenesMEX3D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578304
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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