A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645447



Internal ID7032197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18839192..18955438hg38UCSC Ensembl
chr20:18819836..18936082hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38116247
hg19116247
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv777e214
Supporting Variantsessv16154942, essv16154940, essv16154941, essv16154938, essv16154939
SamplesHG02016, NA18614, HG02513, NA19454, NA19786
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645447
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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