A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3330256



Internal ID15177244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22619044..22619063hg38UCSC Ensembl
Innerchr20:22619040..22619067hg38UCSC Ensembl
Outerchr20:22619021..22619086hg38UCSC Ensembl
chr20:22599682..22599701hg19UCSC Ensembl
Innerchr20:22599678..22599705hg19UCSC Ensembl
Outerchr20:22599659..22599724hg19UCSC Ensembl
chr20:22547682..22547701hg18UCSC Ensembl
Innerchr20:22547705..22547678hg18UCSC Ensembl
Outerchr20:22547659..22547724hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9678880
SamplesNA12234
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3330256
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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