A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6476308



Internal ID9320657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:73830896..73833358hg38UCSC Ensembl
Outerchr11:73830859..73833408hg38UCSC Ensembl
Innerchr11:73541941..73544403hg19UCSC Ensembl
Outerchr11:73541904..73544453hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382550
hg192550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676629
Supporting Variants
SamplesNA18511
Known GenesMRPL48
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6476308
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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