A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096069



Internal ID21292937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51749793..51752829hg38UCSC Ensembl
Innerchr15:52041990..52045026hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg383037
hg193037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113244
Supporting Variants
Samplessample93
Known GenesLYSMD2, TMOD2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096069
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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