A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664171



Internal ID9583590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85192793..85201021hg38UCSC Ensembl
Outerchr16:85192756..85201071hg38UCSC Ensembl
Innerchr16:85226399..85234627hg19UCSC Ensembl
Outerchr16:85226362..85234677hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg388316
hg198316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6279139
SamplesHG00309
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664171
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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