A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578627



Internal ID16366036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12580521..12586517hg38UCSC Ensembl
Innerchr19:12691335..12697331hg19UCSC Ensembl
Innerchr19:12552335..12558331hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385997
hg195997
hg185997
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6270n54
Supporting Variantsnssv893565, nssv893566
Samples
Known GenesZNF490
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578627
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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