A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667364



Internal ID9933469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69670842..69671876hg38UCSC Ensembl
chr10:71430598..71431632hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381035
hg191035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5884079
SamplesNA19004
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667364
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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