A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1416e214



Internal ID22757310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124855007..124959700hg38UCSC Ensembl
chr8:125867249..125971942hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38104694
hg19104694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3618705, esv3618706
SamplesNA19917, HG00123
Known GenesLINC00964
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1416e214
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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