A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752620



Internal ID18380180
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 StatusS
Merged Variantsesv3553873
Supporting Variants
Samples
Known GenesZC3H18
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752620
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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