A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14233458



Internal ID3699807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91499589..91546648hg38UCSC Ensembl
Innerchr11:91499589..91546648hg38UCSC Ensembl
Outerchr11:91499089..91547148hg38UCSC Ensembl
chr11:91232755..91279814hg19UCSC Ensembl
Innerchr11:91232755..91279814hg19UCSC Ensembl
Outerchr11:91232255..91280314hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3847060
hg1947060
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627251
Supporting Variants
SamplesHG03301
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14233458
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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