A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5863143



Internal ID8840546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:146483723..146485927hg38UCSC Ensembl
Outerchr5:146483686..146485977hg38UCSC Ensembl
Innerchr5:145863286..145865490hg19UCSC Ensembl
Outerchr5:145863249..145865540hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382292
hg192292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677262
Supporting Variants
SamplesNA19473
Known GenesTCERG1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5863143
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