A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662152



Internal ID9928257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160823387..160825342hg38UCSC Ensembl
chr1:160793177..160795132hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg381956
hg191956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5490739
SamplesHG00692
Known GenesLY9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662152
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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