A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv934e214



Internal ID18981109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131361494..131382962hg38UCSC Ensembl
chr3:131080338..131101806hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3821469
hg1921469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3597787, esv3597789
SamplesHG02968
Known GenesLOC339874, NUDT16, NUDT16P1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv934e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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