A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656526



Internal ID9922631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110144074..110146462hg38UCSC Ensembl
Outerchr10:110144037..110146512hg38UCSC Ensembl
Innerchr10:111903832..111906220hg19UCSC Ensembl
Outerchr10:111903795..111906270hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382476
hg192476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5664351
SamplesNA20519
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656526
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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