A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6242596



Internal ID9648637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95150494..95150968hg38UCSC Ensembl
Outerchr11:95150337..95151121hg38UCSC Ensembl
Innerchr11:94883658..94884132hg19UCSC Ensembl
Outerchr11:94883501..94884285hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2669678
Supporting Variants
SamplesNA19380
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6242596
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