A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv927e199



Internal ID22758700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24339398..24342200hg38UCSC Ensembl
chr4:24341021..24343823hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382803
hg192803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2664738, esv2669238
SamplesHG00237
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv927e199
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