A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579350



Internal ID16020073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34481093..34482419hg38UCSC Ensembl
Innerchr19:34971998..34973324hg19UCSC Ensembl
Innerchr19:39663838..39665164hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381327
hg191327
hg181327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6408n54
Supporting Variantsnssv898580, nssv898581
Samples
Known GenesWTIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579350
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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