A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662141



Internal ID9928246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43490744..43492552hg38UCSC Ensembl
Outerchr10:43490587..43492705hg38UCSC Ensembl
Innerchr10:43986192..43988000hg19UCSC Ensembl
Outerchr10:43986035..43988153hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382119
hg192119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5664589, essv6048348, essv5893387, essv5761864, essv5951053, essv6283186
SamplesHG01366, NA19904, NA18520, NA19449, NA19712, NA19474
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662141
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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