A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv100e214



Internal ID22755994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18089598..18118169hg38UCSC Ensembl
chr10:18378527..18407098hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3828572
hg1928572
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3622500, esv3622501
SamplesHG00179, NA12813, HG00383
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv100e214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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