A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13665656



Internal ID3667472
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622101
Supporting Variants
SamplesHG02549
Known GenesADARB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13665656
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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