A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5908320



Internal ID9862900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11205716..11208611hg38UCSC Ensembl
chr16:11299573..11302468hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg382896
hg192896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659112
Supporting Variants
SamplesNA20533
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5908320
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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