A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096500



Internal ID21281914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10322775..10362649hg38UCSC Ensembl
Innerchr16:10416632..10456506hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3839875
hg1939875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118024
Supporting Variants
Samplessample319
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096500
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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