A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751782



Internal ID18726028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4084285..4091136hg38UCSC Ensembl
Outerchr16:4083500..4091499hg38UCSC Ensembl
Innerchr16:4134286..4141137hg19UCSC Ensembl
Outerchr16:4133501..4141500hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553035
Supporting Variants
Samples
Known GenesADCY9
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751782
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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