A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642185



Internal ID7028955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34233913..34235349hg38UCSC Ensembl
Innerchr18:34233963..34235299hg38UCSC Ensembl
Outerchr18:34233863..34235399hg38UCSC Ensembl
chr18:31813877..31815313hg19UCSC Ensembl
Innerchr18:31813927..31815263hg19UCSC Ensembl
Outerchr18:31813827..31815363hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381437
hg191437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15839510, essv15839509
SamplesNA19020, NA18870
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642185
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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