A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6252607



Internal ID9230010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:749209..753048hg38UCSC Ensembl
Outerchr11:749052..753201hg38UCSC Ensembl
Innerchr11:749209..753048hg19UCSC Ensembl
Outerchr11:749052..753201hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384150
hg194150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661152
Supporting Variants
SamplesNA18637
Known GenesTALDO1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6252607
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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