A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751773



Internal ID18726019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3469456..3469614hg38UCSC Ensembl
Outerchr16:3469423..3469653hg38UCSC Ensembl
Innerchr16:3519456..3519614hg19UCSC Ensembl
Outerchr16:3519423..3519653hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553026
Supporting Variants
Samples
Known GenesNAA60
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751773
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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