A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv101e214



Internal ID22755995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18771890..18980142hg38UCSC Ensembl
chr10:19060819..19269071hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38208253
hg19208253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3622519, esv3622518
SamplesNA19378, NA19334
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv101e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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