A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1399e214



Internal ID22757293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55071328..55094385hg38UCSC Ensembl
chr8:55983888..56006945hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3823058
hg1923058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3617271, esv3617270
SamplesNA20586, NA19461, NA20763
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1399e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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