A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663990



Internal ID9583409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28020015..28947419hg38UCSC Ensembl
Outerchr19:28019981..28947454hg38UCSC Ensembl
Innerchr19:28510922..29438326hg19UCSC Ensembl
Outerchr19:28510888..29438361hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38927474
hg19927474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6003509
SamplesNA12287
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663990
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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