A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641836



Internal ID6681918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12364101..12364654hg38UCSC Ensembl
Innerchr18:12364107..12364649hg38UCSC Ensembl
Outerchr18:12364096..12364660hg38UCSC Ensembl
chr18:12364100..12364653hg19UCSC Ensembl
Innerchr18:12364106..12364648hg19UCSC Ensembl
Outerchr18:12364095..12364659hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15811121
SamplesHG04161
Known GenesAFG3L2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641836
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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