A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097027



Internal ID21277080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71689972..71698228hg38UCSC Ensembl
Innerchr15:71982311..71990567hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg388257
hg198257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110506
Supporting Variants
Samplessample245
Known GenesTHSD4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097027
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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