A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5792576



Internal ID9761315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60047022..60064591hg38UCSC Ensembl
Outerchr16:60046985..60064641hg38UCSC Ensembl
Innerchr16:60080926..60098495hg19UCSC Ensembl
Outerchr16:60080889..60098545hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3817657
hg1917657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666048
Supporting Variants
SamplesNA19716
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5792576
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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