A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6006394



Internal ID9141407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68258947..68260585hg38UCSC Ensembl
Outerchr10:68258910..68260635hg38UCSC Ensembl
Innerchr10:70018704..70020342hg19UCSC Ensembl
Outerchr10:70018667..70020392hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381726
hg191726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667222
Supporting Variants
SamplesHG01188
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6006394
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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