A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099234



Internal ID21274038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83881963..83948837hg38UCSC Ensembl
Innerchr16:83915568..83982442hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3866875
hg1966875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114141
Supporting Variants
Samplessample200
Known GenesMLYCD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099234
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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