A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16154266



Internal ID4650920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17877540..17879130hg38UCSC Ensembl
Innerchr20:17877578..17879093hg38UCSC Ensembl
Outerchr20:17877503..17879168hg38UCSC Ensembl
chr20:17858184..17859774hg19UCSC Ensembl
Innerchr20:17858222..17859737hg19UCSC Ensembl
Outerchr20:17858147..17859812hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg381591
hg191591
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645431
Supporting Variants
SamplesHG04180
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16154266
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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