A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622101



Internal ID6662271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1327809..1419906hg38UCSC Ensembl
chr10:1370004..1462101hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3892098
hg1992098
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13665657, essv13665656
SamplesHG02549, HG03063
Known GenesADARB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622101
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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