A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660543



Internal ID9926648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32406076..32406368hg38UCSC Ensembl
chr1:32871677..32871969hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5800506, essv6042259, essv5881366, essv6150232, essv6195180, essv5728274
SamplesNA19374, NA18874, NA19707, NA19390, NA19834, NA19835
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660543
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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