A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662064



Internal ID9928169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:49765053..49800268hg38UCSC Ensembl
Outerchr16:49765016..49800318hg38UCSC Ensembl
Innerchr16:49798964..49834179hg19UCSC Ensembl
Outerchr16:49798927..49834229hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3835303
hg1935303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5609290
SamplesHG01149
Known GenesZNF423
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662064
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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