A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6219635



Internal ID9197038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89732697..89732883hg38UCSC Ensembl
chr16:89799105..89799291hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672413
Supporting Variants
SamplesNA18990
Known GenesZNF276
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6219635
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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