A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642012



Internal ID7028782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25898734..25925579hg38UCSC Ensembl
Innerchr18:25898734..25925579hg38UCSC Ensembl
Outerchr18:25898644..25925730hg38UCSC Ensembl
chr18:23478698..23505543hg19UCSC Ensembl
Innerchr18:23478698..23505543hg19UCSC Ensembl
Outerchr18:23478608..23505694hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3826846
hg1926846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv607e214
Supporting Variantsessv15822114, essv15822115
SamplesHG02323, HG00637
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642012
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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