A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578642



Internal ID16019365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14028192..14187630hg38UCSC Ensembl
Innerchr19:14139004..14298442hg19UCSC Ensembl
Innerchr19:14000004..14159442hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38159439
hg19159439
hg18159439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv894812
Samples
Known GenesASF1B, C19orf67, IL27RA, LOC100507373, LOC113230, LPHN1, MIR1199, PALM3, PRKACA, RLN3, SAMD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578642
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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