A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5815774



Internal ID9699511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11745115..11751999hg38UCSC Ensembl
chr20:11725763..11732647hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg386885
hg196885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672392
Supporting Variants
SamplesNA19449
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5815774
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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