A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095952



Internal ID21282619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60590916..60594248hg38UCSC Ensembl
Innerchr15:60883115..60886447hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg383333
hg193333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111436
Supporting Variants
Samplessample33
Known GenesRORA
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095952
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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