A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661088



Internal ID9580507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:88720122..88721820hg38UCSC Ensembl
Outerchr10:88720085..88721870hg38UCSC Ensembl
Innerchr10:90479879..90481577hg19UCSC Ensembl
Outerchr10:90479842..90481627hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg381786
hg191786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6196048
SamplesNA18487
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661088
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