A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv99e214



Internal ID22755993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17567393..17588332hg38UCSC Ensembl
chr10:17609392..17630331hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3820940
hg1920940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3622491, esv3622492
SamplesHG01848, HG02512, HG02141
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv99e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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