A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589668



Internal ID6976997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3845918..3926443hg38UCSC Ensembl
Innerchr2:3845928..3926434hg38UCSC Ensembl
Outerchr2:3845909..3926453hg38UCSC Ensembl
chr2:3893508..3974033hg19UCSC Ensembl
Innerchr2:3893518..3974024hg19UCSC Ensembl
Outerchr2:3893499..3974043hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3880526
hg1980526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10399570
SamplesHG02374
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589668
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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