A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658677



Internal ID9924782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10633126..10636107hg38UCSC Ensembl
Outerchr16:10633089..10636157hg38UCSC Ensembl
Innerchr16:10726983..10729964hg19UCSC Ensembl
Outerchr16:10726946..10730014hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg383069
hg193069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6422989
SamplesHG01462
Known GenesTEKT5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658677
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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