A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669368



Internal ID9588787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42606561..42612753hg38UCSC Ensembl
chr10:43102009..43108201hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg386193
hg196193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6210880
SamplesNA19390
Known GenesZNF33B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669368
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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