A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111970



Internal ID21295236
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 StatusM
Merged Variants
Supporting Variantsnssv14098214
Samplessample7
Known GenesGGA2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111970
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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