A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660476



Internal ID9926581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101258858..101264676hg38UCSC Ensembl
Outerchr10:101258821..101264726hg38UCSC Ensembl
Innerchr10:103018615..103024433hg19UCSC Ensembl
Outerchr10:103018578..103024483hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg385906
hg195906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6426833
SamplesNA06984
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660476
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