A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6517108



Internal ID9494511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68034914..68035746hg38UCSC Ensembl
Outerchr11:68034757..68035899hg38UCSC Ensembl
Innerchr11:67802381..67803213hg19UCSC Ensembl
Outerchr11:67802224..67803366hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381143
hg191143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672926
Supporting Variants
SamplesHG00560
Known GenesNDUFS8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6517108
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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