A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10948008



Internal ID3246608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21806267..21816678hg38UCSC Ensembl
Innerchr3:21806767..21816178hg38UCSC Ensembl
Outerchr3:21805267..21817678hg38UCSC Ensembl
chr3:21847759..21858170hg19UCSC Ensembl
Innerchr3:21848259..21857670hg19UCSC Ensembl
Outerchr3:21846759..21859170hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3810412
hg1910412
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595524
Supporting Variants
SamplesHG02860
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10948008
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