A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099143



Internal ID21270604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23033891..23037519hg38UCSC Ensembl
Innerchr16:23045212..23048840hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg383629
hg193629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110688
Supporting Variants
Samplessample153
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099143
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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