A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641855



Internal ID7028626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13465839..13466876hg38UCSC Ensembl
Innerchr18:13465846..13466869hg38UCSC Ensembl
Outerchr18:13465832..13466883hg38UCSC Ensembl
chr18:13465838..13466875hg19UCSC Ensembl
Innerchr18:13465845..13466868hg19UCSC Ensembl
Outerchr18:13465831..13466882hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381038
hg191038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15812647
SamplesNA18486
Known GenesLDLRAD4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641855
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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