A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv197e215



Internal ID20151236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10462375..10462678hg38UCSC Ensembl
chr18:10462372..10462675hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3555048, esv3555049
Samples
Known GenesAPCDD1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)dgv197e215
Frequency
Sample Size767
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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