A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv864e214



Internal ID20122287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4084346..4218932hg38UCSC Ensembl
chr3:4126030..4260616hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38134587
hg19134587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3595087, esv3595083
SamplesHG01985, HG00766, NA18877, HG02600, HG03518, NA19098, HG03199, HG03986, HG01046, NA19385, HG03814, HG02427, NA18557, NA19327, HG02221, NA20903, HG02256, NA20542, HG03934, NA19019, HG03433, NA19779, HG00728, NA20502, HG03890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv864e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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