A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097544



Internal ID21274899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51752733..51754471hg38UCSC Ensembl
Innerchr15:52044930..52046668hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg381739
hg191739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111305
Supporting Variants
Samplessample214
Known GenesTMOD2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097544
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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