A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659722



Internal ID9925827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:14528096..14534007hg38UCSC Ensembl
Outerchr5:14527939..14534160hg38UCSC Ensembl
Innerchr5:14528205..14534116hg19UCSC Ensembl
Outerchr5:14528048..14534269hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg386222
hg196222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5936624
SamplesHG00699
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659722
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