A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642201



Internal ID7028971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35402118..35408146hg38UCSC Ensembl
Innerchr18:35402118..35408146hg38UCSC Ensembl
Outerchr18:35401880..35408413hg38UCSC Ensembl
chr18:32982082..32988110hg19UCSC Ensembl
Innerchr18:32982082..32988110hg19UCSC Ensembl
Outerchr18:32981844..32988377hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg386029
hg196029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842021
SamplesHG00672
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642201
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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