A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642024



Internal ID7028794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26727563..26731181hg38UCSC Ensembl
Innerchr18:26727563..26731181hg38UCSC Ensembl
Outerchr18:26727365..26731361hg38UCSC Ensembl
chr18:24307527..24311145hg19UCSC Ensembl
Innerchr18:24307527..24311145hg19UCSC Ensembl
Outerchr18:24307329..24311325hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383619
hg193619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15824371, essv15824370
SamplesHG01271, HG00473
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642024
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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