A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579196



Internal ID16019919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27709380..28519597hg38UCSC Ensembl
Innerchr19:28200288..29010504hg19UCSC Ensembl
Innerchr19:32892128..33702344hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38810218
hg19810217
hg18810217
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv897315
Samples
Known GenesLINC00662
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579196
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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