A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5540954



Internal ID9759299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19734698..19946310hg38UCSC Ensembl
Outerchr21:19734664..19946345hg38UCSC Ensembl
Innerchr21:21107012..21318624hg19UCSC Ensembl
Outerchr21:21106978..21318659hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38211682
hg19211682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657283
Supporting Variants
SamplesNA19713
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5540954
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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