A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646707



Internal ID7033450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25398992..25415042hg38UCSC Ensembl
chr21:26771304..26787354hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg3816051
hg1916051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16296829
SamplesNA19401
Known GenesLINC00158
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646707
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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