A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv903e214



Internal ID22756797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:76673696..76759047hg38UCSC Ensembl
chr3:76722847..76808198hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3885352
hg1985352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3596644, esv3596645
SamplesHG03240
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv903e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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