A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675297



Internal ID9941402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15508251..15514992hg38UCSC Ensembl
Outerchr11:15508217..15515027hg38UCSC Ensembl
Innerchr11:15529797..15536538hg19UCSC Ensembl
Outerchr11:15529763..15536573hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg386811
hg196811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5419603
SamplesHG00436
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675297
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