A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096167



Internal ID21270329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51749793..51756215hg38UCSC Ensembl
Innerchr15:52041990..52048412hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg386423
hg196423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116940
Supporting Variants
Samplessample149
Known GenesLYSMD2, TMOD2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096167
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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