A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091362



Internal ID21280446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:219696378..219699951hg38UCSC Ensembl
Innerchr1:219869720..219873293hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg383574
hg193574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115461
Supporting Variants
Samplessample299
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091362
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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