A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106931



Internal ID21287605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:143198687..143283240hg38UCSC Ensembl
Innerchr2:143956256..144040809hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg3884554
hg1984554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110389
Supporting Variants
Samplessample403
Known GenesARHGAP15
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106931
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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