A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666662



Internal ID9586081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162289243..162342465hg38UCSC Ensembl
Outerchr6:162289206..162342515hg38UCSC Ensembl
Innerchr6:162710275..162763497hg19UCSC Ensembl
Outerchr6:162710238..162763547hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3853310
hg1953310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6239456
SamplesHG00176
Known GenesPARK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666662
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