A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv577e199



Internal ID20123879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3504050..3507531hg38UCSC Ensembl
chr18:3504048..3507529hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383482
hg193482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2675244, esv2669851
SamplesNA11994
Known GenesDLGAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv577e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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