A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5813642



Internal ID8791045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:16278036..16278860hg38UCSC Ensembl
Outerchr19:16277999..16278910hg38UCSC Ensembl
Innerchr19:16388847..16389671hg19UCSC Ensembl
Outerchr19:16388810..16389721hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38912
hg19912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2673595
Supporting Variants
SamplesNA19916
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5813642
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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