A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089914



Internal ID21278317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196758704..196832286hg38UCSC Ensembl
Innerchr1:196727834..196801416hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3873583
hg1973583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110553
Supporting Variants
Samplessample268
Known GenesCFHR1, CFHR3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089914
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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