A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095287



Internal ID21266594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51748653..51754471hg38UCSC Ensembl
Innerchr15:52040850..52046668hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg385819
hg195819
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115616
Supporting Variants
Samplessample10
Known GenesLYSMD2, TMOD2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095287
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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