A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3306874



Internal ID15153822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19200217..19200218hg38UCSC Ensembl
Innerchr20:19200195..19200240hg38UCSC Ensembl
Outerchr20:19200194..19200241hg38UCSC Ensembl
chr20:19180861..19180862hg19UCSC Ensembl
Innerchr20:19180839..19180884hg19UCSC Ensembl
Outerchr20:19180838..19180885hg19UCSC Ensembl
chr20:19128861..19128862hg18UCSC Ensembl
Innerchr20:19128884..19128839hg18UCSC Ensembl
Outerchr20:19128838..19128885hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38288
hg19288
hg18288
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7769433
SamplesNA19141
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3306874
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer