A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645596



Internal ID7032345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25731016..25742904hg38UCSC Ensembl
chr20:25711652..25723540hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3811889
hg1911889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16166655, essv16166657, essv16166659, essv16166656, essv16166661, essv16166662, essv16166654, essv16166660, essv16166652, essv16166653, essv16166658
SamplesNA18745, HG00351, NA19734, HG01277, HG00355, HG00130, NA19451, HG02090, HG02497, NA19735, NA19435
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645596
Frequency
Sample Size2504
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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