A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv162e214



Internal ID22756056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97813677..97827265hg38UCSC Ensembl
chr10:99573434..99587022hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3813589
hg1913589
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3624324, esv3624323
SamplesNA11933, NA19355, NA19457
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv162e214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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