A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6541288



Internal ID9733589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:4352695..4354566hg38UCSC Ensembl
Outerchr4:4352538..4354719hg38UCSC Ensembl
Innerchr4:4354422..4356293hg19UCSC Ensembl
Outerchr4:4354265..4356446hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg382182
hg192182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668657
Supporting Variants
SamplesNA19660
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6541288
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer