A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642675



Internal ID7029444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59812168..59824081hg38UCSC Ensembl
Innerchr18:59812201..59824048hg38UCSC Ensembl
Outerchr18:59812135..59824114hg38UCSC Ensembl
chr18:57479400..57491313hg19UCSC Ensembl
Innerchr18:57479433..57491280hg19UCSC Ensembl
Outerchr18:57479367..57491346hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3811914
hg1911914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15897067
SamplesHG03914
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642675
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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