A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622106



Internal ID6662276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1571478..1575138hg38UCSC Ensembl
chr10:1613673..1617333hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg383661
hg193661
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13665698, essv13665702, essv13665699, essv13665701, essv13665700
SamplesHG01188, NA20755, HG02090, NA12348, HG02067
Known GenesADARB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622106
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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