A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112653



Internal ID21295919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:25003836..25007655hg38UCSC Ensembl
Innerchr16:25015157..25018976hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg383820
hg193820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096434
Samplessample283
Known GenesARHGAP17
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112653
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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