A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6090816



Internal ID9068219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8936537..8943612hg38UCSC Ensembl
Outerchr11:8936500..8943662hg38UCSC Ensembl
Innerchr11:8958084..8965159hg19UCSC Ensembl
Outerchr11:8958047..8965209hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387163
hg197163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678695
Supporting Variants
SamplesNA18622
Known GenesASCL3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6090816
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