A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv991e214



Internal ID22756885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18930034..18994505hg38UCSC Ensembl
chr4:18931657..18996128hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3864472
hg1964472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3599806, esv3599805
SamplesNA20274, HG01607
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv991e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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