A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622105



Internal ID6662275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1571478..1575138hg38UCSC Ensembl
chr10:1613673..1617333hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg383661
hg193661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13665696, essv13665694, essv13665695, essv13665697
SamplesHG01456, HG03913, HG00320, NA18853
Known GenesADARB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622105
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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