A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15869686



Internal ID5426952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:51651408..51669094hg38UCSC Ensembl
chr18:49177778..49195464hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3817687
hg1917687
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642527
Supporting Variants
SamplesNA18953
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15869686
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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