A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578661



Internal ID16019384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14090741..14092730hg38UCSC Ensembl
Innerchr19:14201553..14203542hg19UCSC Ensembl
Innerchr19:14062553..14064542hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381990
hg191990
hg181990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv894840
Samples
Known GenesPRKACA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578661
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer