A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv21e214



Internal ID22755915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55795000..55833319hg38UCSC Ensembl
chr1:56260673..56298992hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3838320
hg1938320
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3586116, esv3586117
SamplesHG02073, HG02019, HG01600
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv21e214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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