A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5582793



Internal ID8818766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68452138..68453498hg38UCSC Ensembl
chr10:70211895..70213255hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381361
hg191361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675728
Supporting Variants
SamplesHG00260
Known GenesDNA2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5582793
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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