A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6034790



Internal ID9012193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22897652..22897930hg38UCSC Ensembl
chr16:22908973..22909251hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661611
Supporting Variants
SamplesNA18945
Known GenesHS3ST2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6034790
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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