A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667578



Internal ID9933683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83126526..83135086hg38UCSC Ensembl
chr11:82837568..82846128hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg388561
hg198561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6419415, essv5870778, essv6432673, essv5639640, essv6419157, essv6069209
SamplesHG01066, NA20816, HG00139, HG00319, HG00269, HG01491
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667578
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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