A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596492



Internal ID6983807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69117853..69155083hg38UCSC Ensembl
Innerchr3:69117899..69155037hg38UCSC Ensembl
Outerchr3:69117807..69155129hg38UCSC Ensembl
chr3:69167004..69204234hg19UCSC Ensembl
Innerchr3:69167050..69204188hg19UCSC Ensembl
Outerchr3:69166958..69204280hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3837231
hg1937231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11035672
SamplesNA21144
Known GenesLMOD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596492
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