A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6573163



Internal ID9153695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92159167..92162203hg38UCSC Ensembl
Outerchr15:92159118..92162253hg38UCSC Ensembl
Innerchr15:92702397..92705433hg19UCSC Ensembl
Outerchr15:92702348..92705483hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383136
hg193136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677093
Supporting Variants
SamplesHG01342
Known GenesSLCO3A1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6573163
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