A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093261



Internal ID21278478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:234887222..234894590hg38UCSC Ensembl
Innerchr1:235022969..235030337hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg387369
hg197369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112748
Supporting Variants
Samplessample27
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093261
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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