A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14089287



Internal ID4091103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34476653..34498139hg38UCSC Ensembl
Innerchr11:34476653..34498139hg38UCSC Ensembl
Outerchr11:34476153..34498639hg38UCSC Ensembl
chr11:34498200..34519686hg19UCSC Ensembl
Innerchr11:34498200..34519686hg19UCSC Ensembl
Outerchr11:34497700..34520186hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3821487
hg1921487
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625912
Supporting Variants
SamplesHG03432
Known GenesELF5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14089287
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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