A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586672



Internal ID6974190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84796869..84797982hg38UCSC Ensembl
Innerchr1:84796885..84797966hg38UCSC Ensembl
Outerchr1:84796853..84797998hg38UCSC Ensembl
chr1:85262552..85263665hg19UCSC Ensembl
Innerchr1:85262568..85263649hg19UCSC Ensembl
Outerchr1:85262536..85263681hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381114
hg191114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10001824
SamplesNA19783
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586672
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