A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv897037



Internal ID16190993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27287920..27783601hg38UCSC Ensembl
Innerchr19:27778828..28274509hg19UCSC Ensembl
Innerchr19:32470668..32966349hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38495682
hg19495682
hg18495682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579127
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv897037
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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