A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578952



Internal ID16366361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21352905..21685782hg38UCSC Ensembl
Innerchr19:21535707..21868584hg19UCSC Ensembl
Innerchr19:21327547..21660424hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38332878
hg19332878
hg18332878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv896581
Samples
Known GenesLINC00664, ZNF429, ZNF493, ZNF738
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578952
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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