A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3553873



Internal ID18408263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88572727..88575700hg38UCSC Ensembl
Outerchr16:88572268..88576494hg38UCSC Ensembl
Innerchr16:88639135..88642108hg19UCSC Ensembl
Outerchr16:88638676..88642902hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg384227
hg194227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9752620
Samples
Known GenesZC3H18
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3553873
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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