A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6422989



Internal ID9188410
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 Flag1
Merged StatusS
Merged Variantsesv2658677
Supporting Variants
SamplesHG01462
Known GenesTEKT5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6422989
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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