A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670021



Internal ID4714355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:64167635..64173475hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv6380491, essv5791859
SamplesNA19471, NA19835
Known GenesZNF365
Method
Analysis
Platform
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670021
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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