A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641727



Internal ID7028498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8843309..8847634hg38UCSC Ensembl
Innerchr18:8843342..8847601hg38UCSC Ensembl
Outerchr18:8843276..8847667hg38UCSC Ensembl
chr18:8843307..8847632hg19UCSC Ensembl
Innerchr18:8843340..8847599hg19UCSC Ensembl
Outerchr18:8843274..8847665hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg384326
hg194326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15795096
SamplesNA18561
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641727
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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