A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579403



Internal ID16020126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35360012..35372038hg38UCSC Ensembl
Innerchr19:35850914..35862940hg19UCSC Ensembl
Innerchr19:40542754..40554780hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812027
hg1912027
hg1812027
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6420n54
Supporting Variantsnssv898786
Samples
Known GenesFFAR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579403
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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