A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5882791



Internal ID8860194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:5057215..5061264hg38UCSC Ensembl
chr16:5107216..5111265hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384050
hg194050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv2667914
Supporting Variants
SamplesHG00651
Known GenesC16orf89
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5882791
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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