A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656730



Internal ID9922835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43212019..43212480hg38UCSC Ensembl
Outerchr10:43211841..43212679hg38UCSC Ensembl
Innerchr10:43707467..43707928hg19UCSC Ensembl
Outerchr10:43707289..43708127hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38839
hg19839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6086055
SamplesNA18523
Known GenesRASGEF1A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656730
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