A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14241836



Internal ID4673969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94375659..94387920hg38UCSC Ensembl
Innerchr11:94375659..94387920hg38UCSC Ensembl
Outerchr11:94375159..94388420hg38UCSC Ensembl
chr11:94108825..94121086hg19UCSC Ensembl
Innerchr11:94108825..94121086hg19UCSC Ensembl
Outerchr11:94108325..94121586hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3812262
hg1912262
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627321
Supporting Variants
SamplesHG04200
Known GenesGPR83
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14241836
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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