A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107261



Internal ID21266737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196825272..196926784hg38UCSC Ensembl
Innerchr1:196794402..196895914hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38101513
hg19101513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112271
Supporting Variants
Samplessample101
Known GenesCFHR1, CFHR4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107261
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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