A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662292



Internal ID9928397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37571615..37575451hg38UCSC Ensembl
Outerchr20:37571578..37575501hg38UCSC Ensembl
Innerchr20:36200017..36203853hg19UCSC Ensembl
Outerchr20:36199980..36203903hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg383924
hg193924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5587327
SamplesNA19430
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662292
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