A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6527936



Internal ID9293003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:63270287..63271637hg38UCSC Ensembl
Outerchr10:63270231..63271699hg38UCSC Ensembl
Innerchr10:65030047..65031397hg19UCSC Ensembl
Outerchr10:65029991..65031459hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381469
hg191469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658212
Supporting Variants
SamplesNA12829
Known GenesJMJD1C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6527936
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