A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11730724



Internal ID5915502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182364489..182375058hg38UCSC Ensembl
Innerchr4:182364500..182375048hg38UCSC Ensembl
Outerchr4:182364479..182375069hg38UCSC Ensembl
chr4:183285642..183296211hg19UCSC Ensembl
Innerchr4:183285653..183296201hg19UCSC Ensembl
Outerchr4:183285632..183296222hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3810570
hg1910570
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603419
Supporting Variants
SamplesNA19327
Known GenesTENM3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11730724
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