A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670052



Internal ID9936157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45256766..45257422hg38UCSC Ensembl
chr10:45752214..45752870hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6491382, essv5847574
SamplesHG00249, HG00264
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670052
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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