A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5458161



Internal ID9807453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:17494305..17495414hg38UCSC Ensembl
Outerchr19:17494140..17495577hg38UCSC Ensembl
Innerchr19:17605114..17606223hg19UCSC Ensembl
Outerchr19:17604949..17606386hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381438
hg191438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677036
Supporting Variants
SamplesNA19908
Known GenesSLC27A1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5458161
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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