A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3553526



Internal ID18754602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60577958..60579522hg38UCSC Ensembl
Outerchr16:60577825..60579580hg38UCSC Ensembl
Innerchr16:60611862..60613426hg19UCSC Ensembl
Outerchr16:60611729..60613484hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381756
hg191756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9752273
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3553526
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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