A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088458



Internal ID21276543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:38584089..38587287hg38UCSC Ensembl
Innerchr1:39049761..39052959hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383199
hg193199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111568
Supporting Variants
Samplessample238
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088458
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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