A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556152



Internal ID18410542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19930529..19930582hg38UCSC Ensembl
chr19:20041338..20041391hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754899
Samples
Known GenesZNF93
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556152
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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