A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6456267



Internal ID9650240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9482195..9487583hg38UCSC Ensembl
chr11:9503742..9509130hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385389
hg195389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675320
Supporting Variants
SamplesNA19381
Known GenesZNF143
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6456267
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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