A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6376233



Internal ID9353636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89901367..89902730hg38UCSC Ensembl
chr16:89967775..89969138hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665192
Supporting Variants
SamplesNA20811
Known GenesTCF25
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6376233
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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