A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665882



Internal ID9931987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89202626..89248339hg38UCSC Ensembl
Outerchr16:89202592..89248374hg38UCSC Ensembl
Innerchr16:89269034..89314747hg19UCSC Ensembl
Outerchr16:89269000..89314782hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3845783
hg1945783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5692753
SamplesHG00146
Known GenesZNF778
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665882
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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