A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14189794



Internal ID5938580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65683808..65687363hg38UCSC Ensembl
Innerchr11:65684308..65686863hg38UCSC Ensembl
Outerchr11:65682808..65688363hg38UCSC Ensembl
chr11:65451279..65454834hg19UCSC Ensembl
Innerchr11:65451779..65454334hg19UCSC Ensembl
Outerchr11:65450279..65455834hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383556
hg193556
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626676
Supporting Variants
SamplesNA19350
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14189794
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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