A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599204



Internal ID6986252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194543170..194560361hg38UCSC Ensembl
Innerchr3:194543186..194560346hg38UCSC Ensembl
Outerchr3:194543155..194560377hg38UCSC Ensembl
chr3:194263899..194281090hg19UCSC Ensembl
Innerchr3:194263915..194281075hg19UCSC Ensembl
Outerchr3:194263884..194281106hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3817192
hg1917192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11283957, essv11283956
SamplesHG03259, HG02371
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599204
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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