A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1050e214



Internal ID22756944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184972549..184987029hg38UCSC Ensembl
chr4:185893703..185908183hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3814481
hg1914481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3603481, esv3603479
SamplesNA19648
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1050e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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