A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093863



Internal ID21281074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196765230..196851756hg38UCSC Ensembl
Innerchr1:196734360..196820886hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3886527
hg1986527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116799
Supporting Variants
Samplessample306
Known GenesCFHR1, CFHR3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093863
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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