A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv478e214



Internal ID22756372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11924452..11941720hg38UCSC Ensembl
chr16:12018309..12035577hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3817269
hg1917269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3637946, esv3637945
SamplesHG01855, NA18486, NA18516
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv478e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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