A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv64e214



Internal ID20121487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179716874..179766076hg38UCSC Ensembl
chr1:179686009..179735211hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3849203
hg1949203
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3588058, esv3588057
SamplesHG03680, HG03696, NA19917
Known GenesFAM163A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv64e214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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