A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10433271



Internal ID3088850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26153217..26156000hg38UCSC Ensembl
Innerchr2:26153219..26155998hg38UCSC Ensembl
Outerchr2:26153215..26156002hg38UCSC Ensembl
chr2:26376086..26378869hg19UCSC Ensembl
Innerchr2:26376088..26378867hg19UCSC Ensembl
Outerchr2:26376084..26378871hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg382784
hg192784
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3590111
Supporting Variants
SamplesHG02715
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10433271
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