A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095356



Internal ID21269376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:55454072..55461073hg38UCSC Ensembl
Innerchr14:55920790..55927791hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg387002
hg197002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113931
Supporting Variants
Samplessample138
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095356
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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