A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3426491



Internal ID14926762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2933354..2934852hg38UCSC Ensembl
Innerchr19:2933852..2934354hg38UCSC Ensembl
Outerchr19:2932354..2935852hg38UCSC Ensembl
chr19:2933352..2934850hg19UCSC Ensembl
Innerchr19:2933850..2934352hg19UCSC Ensembl
Outerchr19:2932352..2935850hg19UCSC Ensembl
chr19:2884352..2885850hg18UCSC Ensembl
Innerchr19:2885352..2884850hg18UCSC Ensembl
Outerchr19:2883352..2886850hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8691454
SamplesNA19239
Known GenesZNF77
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3426491
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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