A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646729



Internal ID6686786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26179578..26192197hg38UCSC Ensembl
chr21:27551897..27564516hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3812620
hg1912620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16299920
SamplesHG03126
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646729
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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