A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752272



Internal ID18726518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60521629..60538286hg38UCSC Ensembl
Outerchr16:60521316..60539112hg38UCSC Ensembl
Innerchr16:60555533..60572190hg19UCSC Ensembl
Outerchr16:60555220..60573016hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3817797
hg1917797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553525
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752272
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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