A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5671026



Internal ID9255568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:133799025..133800931hg38UCSC Ensembl
Outerchr5:133798654..133801301hg38UCSC Ensembl
Innerchr5:133134716..133136622hg19UCSC Ensembl
Outerchr5:133134345..133136992hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg382648
hg192648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671962
Supporting Variants
SamplesNA12156
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5671026
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