A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670368



Internal ID9936473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:20394762..20398117hg38UCSC Ensembl
Outerchr6:20394605..20398270hg38UCSC Ensembl
Innerchr6:20394993..20398348hg19UCSC Ensembl
Outerchr6:20394836..20398501hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383666
hg193666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6460555, essv5779422
SamplesHG00524, HG00512
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670368
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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