A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098214



Internal ID21291107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23479031..23495728hg38UCSC Ensembl
Innerchr16:23490352..23507049hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3816698
hg1916698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111970
Supporting Variants
Samplessample7
Known GenesGGA2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098214
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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