A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3445872



Internal ID15292822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31985688..31988086hg38UCSC Ensembl
Innerchr20:31986688..31987086hg38UCSC Ensembl
Outerchr20:31984688..31989086hg38UCSC Ensembl
chr20:30573491..30575889hg19UCSC Ensembl
Innerchr20:30574491..30574889hg19UCSC Ensembl
Outerchr20:30572491..30576889hg19UCSC Ensembl
chr20:30037152..30039550hg18UCSC Ensembl
Innerchr20:30038152..30038550hg18UCSC Ensembl
Outerchr20:30036152..30040550hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg382399
hg192399
hg182399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8692537
SamplesNA19239
Known GenesXKR7
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3445872
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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