A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099290



Internal ID21275975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57688020..57693829hg38UCSC Ensembl
Innerchr16:57721932..57727741hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385810
hg195810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115303
Supporting Variants
Samplessample230
Known GenesGPR97
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099290
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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