A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5805403



Internal ID9585492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:140323896..140324238hg38UCSC Ensembl
Outerchr5:140323859..140324288hg38UCSC Ensembl
Innerchr5:139703481..139703823hg19UCSC Ensembl
Outerchr5:139703444..139703873hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677051
Supporting Variants
SamplesNA19190
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5805403
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