A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642207



Internal ID7028977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35768355..35777844hg38UCSC Ensembl
Innerchr18:35768355..35777844hg38UCSC Ensembl
Outerchr18:35768121..35778005hg38UCSC Ensembl
chr18:33348319..33357808hg19UCSC Ensembl
Innerchr18:33348319..33357808hg19UCSC Ensembl
Outerchr18:33348085..33357969hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg389490
hg199490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842030, essv15842032, essv15842031
SamplesHG00122, HG03750, HG03382
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642207
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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