A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6538036



Internal ID8719972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4036318..4036502hg38UCSC Ensembl
Outerchr19:4036267..4036564hg38UCSC Ensembl
Innerchr19:4036316..4036500hg19UCSC Ensembl
Outerchr19:4036265..4036562hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658425
Supporting Variants
SamplesHG00096
Known GenesPIAS4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6538036
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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