A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645556



Internal ID7032305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24670892..24841772hg38UCSC Ensembl
chr20:24651528..24822408hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38170881
hg19170881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16163971, essv16163972, essv16163973
SamplesNA19437, NA19440, HG03539
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645556
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer