A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602698



Internal ID6989731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151970284..151972582hg38UCSC Ensembl
Innerchr4:151970284..151972582hg38UCSC Ensembl
Outerchr4:151969976..151972913hg38UCSC Ensembl
chr4:152891436..152893734hg19UCSC Ensembl
Innerchr4:152891436..152893734hg19UCSC Ensembl
Outerchr4:152891128..152894065hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382299
hg192299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11655053, essv11655043, essv11655051, essv11655048, essv11655050, essv11655047, essv11655044, essv11655052, essv11655045, essv11655049, essv11655046
SamplesNA19684, HG03792, NA20320, HG00236, NA20881, HG01988, HG00734, NA20516, HG00343, HG00252, HG00345
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602698
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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