A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096434



Internal ID21279457
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 StatusS
Merged Variantsnsv3112653
Supporting Variants
Samplessample283
Known GenesARHGAP17
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096434
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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