A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16154885



Internal ID3486902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18638418..18646145hg38UCSC Ensembl
chr20:18619062..18626789hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg387728
hg197728
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645443
Supporting Variants
SamplesHG03099
Known GenesDTD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16154885
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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