A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1263e214



Internal ID22757157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12413845..12456477hg38UCSC Ensembl
chr7:12453471..12496103hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3842633
hg1942633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3612251, esv3612253
SamplesHG04185
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1263e214
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