A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv928e214



Internal ID20122351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119505783..119509080hg38UCSC Ensembl
chr3:119224630..119227927hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg383298
hg193298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3597562, esv3597560
SamplesHG04144, HG03491, HG02660, HG03611
Known GenesTIMMDC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv928e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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