A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579866



Internal ID16367275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:45320405..45323890hg38UCSC Ensembl
Innerchr19:45823663..45827148hg19UCSC Ensembl
Innerchr19:50515503..50518988hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg383486
hg193486
hg183486
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899934
Samples
Known GenesCKM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579866
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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