A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579117



Internal ID16366526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27241092..27246205hg38UCSC Ensembl
Innerchr19:27732000..27737113hg19UCSC Ensembl
Innerchr19:32423840..32428953hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg385114
hg195114
hg185114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6360n54
Supporting Variantsnssv897025
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579117
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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