A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5907502



Internal ID9741566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:47767767..47774938hg38UCSC Ensembl
Outerchr19:47767730..47774988hg38UCSC Ensembl
Innerchr19:48271024..48278195hg19UCSC Ensembl
Outerchr19:48270987..48278245hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg387259
hg197259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660018
Supporting Variants
SamplesNA19678
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5907502
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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