A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095574



Internal ID21275550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:58636713..58640128hg38UCSC Ensembl
Innerchr14:59103431..59106846hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg383416
hg193416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114837
Supporting Variants
Samplessample224
Known GenesDACT1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095574
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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