A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642023



Internal ID7028793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26450512..26452574hg38UCSC Ensembl
Innerchr18:26450563..26452523hg38UCSC Ensembl
Outerchr18:26450461..26452625hg38UCSC Ensembl
chr18:24030476..24032538hg19UCSC Ensembl
Innerchr18:24030527..24032487hg19UCSC Ensembl
Outerchr18:24030425..24032589hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382063
hg192063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15824369, essv15824367, essv15824368
SamplesHG03121, HG01950, NA20509
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642023
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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