A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117179



Internal ID21300445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21246652..21257178hg38UCSC Ensembl
Innerchr16:21257973..21268499hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3810527
hg1910527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099092
Samplessample128
Known GenesANKS4B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117179
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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