A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6471659



Internal ID9351208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36577393..36581063hg38UCSC Ensembl
Outerchr8:36577236..36581216hg38UCSC Ensembl
Innerchr8:36434911..36438581hg19UCSC Ensembl
Outerchr8:36434754..36438734hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg383981
hg193981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661333
Supporting Variants
SamplesNA18546
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6471659
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