A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv921e214



Internal ID20122344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114256209..114297720hg38UCSC Ensembl
chr3:113975056..114016567hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3841512
hg1941512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3597453, esv3597454
SamplesNA21106, NA21118, HG04180, NA21086, HG03809, HG03600, HG03642, HG00628
Known GenesTIGIT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv921e214
Frequency
Sample Size2504
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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