A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6226177



Internal ID9203580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79598419..79600625hg38UCSC Ensembl
Outerchr16:79598048..79600995hg38UCSC Ensembl
Innerchr16:79632316..79634522hg19UCSC Ensembl
Outerchr16:79631945..79634892hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg382948
hg192948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672388
Supporting Variants
SamplesHG01456
Known GenesMAF
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6226177
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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