A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14043398



Internal ID5897067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18642946..18649139hg38UCSC Ensembl
Innerchr11:18643096..18648989hg38UCSC Ensembl
Outerchr11:18642796..18649289hg38UCSC Ensembl
chr11:18664493..18670686hg19UCSC Ensembl
Innerchr11:18664643..18670536hg19UCSC Ensembl
Outerchr11:18664343..18670836hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg386194
hg196194
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625509
Supporting Variants
SamplesNA19316
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14043398
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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