A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113077



Internal ID21296343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87716031..87718241hg38UCSC Ensembl
Innerchr16:87749637..87751847hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382211
hg192211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096463
Samplessample299
Known GenesKLHDC4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113077
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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