A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6469191



Internal ID9364418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122185499..122186668hg38UCSC Ensembl
Outerchr10:122185342..122186821hg38UCSC Ensembl
Innerchr10:123945014..123946183hg19UCSC Ensembl
Outerchr10:123944857..123946336hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381480
hg191480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2666599
Supporting Variants
SamplesNA18559
Known GenesTACC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6469191
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