A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642202



Internal ID7028972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35446899..35449714hg38UCSC Ensembl
Innerchr18:35446923..35449690hg38UCSC Ensembl
Outerchr18:35446875..35449738hg38UCSC Ensembl
chr18:33026863..33029678hg19UCSC Ensembl
Innerchr18:33026887..33029654hg19UCSC Ensembl
Outerchr18:33026839..33029702hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg382816
hg192816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842022
SamplesHG03078
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642202
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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