A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643116



Internal ID7029885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74407165..74409436hg38UCSC Ensembl
Innerchr18:74407186..74409416hg38UCSC Ensembl
Outerchr18:74407145..74409457hg38UCSC Ensembl
chr18:72074400..72076671hg19UCSC Ensembl
Innerchr18:72074421..72076651hg19UCSC Ensembl
Outerchr18:72074380..72076692hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg382272
hg192272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15934073, essv15934074
SamplesNA06984, NA19091
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643116
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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