A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589800



Internal ID6977130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10490337..10535656hg38UCSC Ensembl
chr2:10630463..10675782hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3845320
hg1945320
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10406927
SamplesNA18564
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589800
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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