A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8740988



Internal ID15085676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3798095..3798095hg38UCSC Ensembl
Innerchr20:3798094..3798096hg38UCSC Ensembl
Outerchr20:3798045..3798145hg38UCSC Ensembl
chr20:3778742..3778742hg19UCSC Ensembl
Innerchr20:3778741..3778743hg19UCSC Ensembl
Outerchr20:3778692..3778792hg19UCSC Ensembl
chr20:3726742..3726742hg18UCSC Ensembl
Innerchr20:3726743..3726741hg18UCSC Ensembl
Outerchr20:3726692..3726792hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38668
hg19668
hg18668
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3385581
Supporting Variants
SamplesNA19240
Known GenesCDC25B
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8740988
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