A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597605



Internal ID6984744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122307229..122308126hg38UCSC Ensembl
Innerchr3:122307251..122308104hg38UCSC Ensembl
Outerchr3:122307207..122308148hg38UCSC Ensembl
chr3:122026076..122026973hg19UCSC Ensembl
Innerchr3:122026098..122026951hg19UCSC Ensembl
Outerchr3:122026054..122026995hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38898
hg19898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11123000
SamplesHG01708
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597605
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