A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5937470



Internal ID9656004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8270032..8294038hg38UCSC Ensembl
Outerchr19:8269661..8294408hg38UCSC Ensembl
Innerchr19:8334916..8358922hg19UCSC Ensembl
Outerchr19:8334545..8359292hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3824748
hg1924748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675668
Supporting Variants
SamplesNA19385
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5937470
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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