A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596879



Internal ID6637149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86908792..86940260hg38UCSC Ensembl
Innerchr3:86909292..86939760hg38UCSC Ensembl
Outerchr3:86907792..86941260hg38UCSC Ensembl
chr3:86957942..86989410hg19UCSC Ensembl
Innerchr3:86958442..86988910hg19UCSC Ensembl
Outerchr3:86956942..86990410hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3831469
hg1931469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11063947
SamplesNA21133
Known GenesVGLL3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596879
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