A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085858



Internal ID21274984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:13748078..13751850hg38UCSC Ensembl
Innerchr1:14074573..14078345hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg383773
hg193773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115456
Supporting Variants
Samplessample216
Known GenesPRDM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085858
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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