A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665624



Internal ID9931729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68799747..68802979hg38UCSC Ensembl
chr10:70559504..70562736hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383233
hg193233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5775741, essv5507640
SamplesHG01066, NA19315
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665624
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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