A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1382e214



Internal ID20122805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16087881..16166383hg38UCSC Ensembl
chr8:15945390..16023892hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3878503
hg1978503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3616430, esv3616431
SamplesHG03015, HG00337, HG02687, HG03746
Known GenesMSR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1382e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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