A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5784375



Internal ID9456102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38279165..38283158hg38UCSC Ensembl
Outerchr21:38279128..38283208hg38UCSC Ensembl
Innerchr21:39651087..39655080hg19UCSC Ensembl
Outerchr21:39651050..39655130hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg384081
hg194081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677092
Supporting Variants
SamplesNA18907
Known GenesKCNJ15
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5784375
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