A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv915e214



Internal ID22756809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99052037..99224489hg38UCSC Ensembl
chr3:98770881..98943333hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38172453
hg19172453
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3597130, esv3597133
SamplesHG00592, HG01389, HG02047, HG01432
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv915e214
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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