A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090735



Internal ID21267831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:219696608..219699359hg38UCSC Ensembl
Innerchr1:219869950..219872701hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg382752
hg192752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113223
Supporting Variants
Samplessample117
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090735
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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