A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6121752



Internal ID9528850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68457281..68458088hg38UCSC Ensembl
chr16:68491184..68491991hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38808
hg19808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661660
Supporting Variants
SamplesNA19058
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6121752
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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