A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15909919



Internal ID5459555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:65637666..65638492hg38UCSC Ensembl
Innerchr18:65637668..65638490hg38UCSC Ensembl
Outerchr18:65637664..65638494hg38UCSC Ensembl
chr18:63304902..63305728hg19UCSC Ensembl
Innerchr18:63304904..63305726hg19UCSC Ensembl
Outerchr18:63304900..63305730hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38827
hg19827
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642840
Supporting Variants
SamplesNA18968
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15909919
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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