A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107984



Internal ID21292826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:234274308..234276827hg38UCSC Ensembl
Innerchr1:234410054..234412573hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg382520
hg192520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117465
Supporting Variants
Samplessample92
Known GenesSLC35F3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107984
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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