A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1068e214



Internal ID22756962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3566319..3591058hg38UCSC Ensembl
chr5:3566433..3591172hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3824740
hg1924740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3603858, esv3603857
SamplesHG01121
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1068e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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