A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv65e214



Internal ID22755959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182330045..182350555hg38UCSC Ensembl
chr1:182299180..182319690hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3820511
hg1920511
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3588100, esv3588101
SamplesNA19456, HG01912, HG01556
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv65e214
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