A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15842010



Internal ID4335418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35214122..35217623hg38UCSC Ensembl
Innerchr18:35214162..35217584hg38UCSC Ensembl
Outerchr18:35214083..35217663hg38UCSC Ensembl
chr18:32794086..32797587hg19UCSC Ensembl
Innerchr18:32794126..32797548hg19UCSC Ensembl
Outerchr18:32794047..32797627hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg383502
hg193502
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642196
Supporting Variants
SamplesHG03875
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15842010
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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