A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083429



Internal ID21273231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:166576409..166646783hg38UCSC Ensembl
Innerchr1:166545646..166616020hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3870375
hg1970375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113565
Supporting Variants
Samplessample189
Known GenesFMO9P
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083429
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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