A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv474e214



Internal ID22756368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3069789..3083133hg38UCSC Ensembl
chr16:3119790..3133134hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3813345
hg1913345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3637650, esv3637649
SamplesHG01965, NA20808, NA12748, HG01512, HG01589, HG01342, NA20510, NA19074
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv474e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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