A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668028



Internal ID9587447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3612264..3634219hg38UCSC Ensembl
Outerchr16:3612227..3634269hg38UCSC Ensembl
Innerchr16:3662265..3684220hg19UCSC Ensembl
Outerchr16:3662228..3684270hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3822043
hg1922043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5964127
SamplesHG01389
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668028
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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