A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5754584



Internal ID9748450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61991844..61992405hg38UCSC Ensembl
Outerchr11:61991807..61992455hg38UCSC Ensembl
Innerchr11:61759316..61759877hg19UCSC Ensembl
Outerchr11:61759279..61759927hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673103
Supporting Variants
SamplesNA19700
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5754584
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