A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6154961



Internal ID8987846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:13906930..13907697hg38UCSC Ensembl
Outerchr11:13906773..13907850hg38UCSC Ensembl
Innerchr11:13928477..13929244hg19UCSC Ensembl
Outerchr11:13928320..13929397hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381078
hg191078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678413
Supporting Variants
SamplesHG00583
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6154961
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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