A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1084e214



Internal ID22756978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28640392..28729684hg38UCSC Ensembl
chr5:28640499..28729791hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3889293
hg1989293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3604515, esv3604514
SamplesHG02122, HG02136, HG04162, HG02379
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1084e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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