A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3553227



Internal ID18407617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:22897656..22897914hg38UCSC Ensembl
Outerchr16:22897607..22897977hg38UCSC Ensembl
Innerchr16:22908977..22909235hg19UCSC Ensembl
Outerchr16:22908928..22909298hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9751974
Samples
Known GenesHS3ST2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3553227
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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