A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670021



Internal ID2903108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62407876..62413716hg38UCSC Ensembl
chr10:64167635..64173475hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg385841
hg195841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6380491, essv5791859
SamplesNA19471, NA19835
Known GenesZNF365
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
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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