A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091176



Internal ID21278674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:233995479..233999064hg38UCSC Ensembl
Innerchr1:234131225..234134810hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg383586
hg193586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115924
Supporting Variants
Samplessample272
Known GenesSLC35F3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091176
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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