A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086819



Internal ID21274510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:24501990..24503802hg38UCSC Ensembl
Innerchr1:24828480..24830292hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381813
hg191813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115036
Supporting Variants
Samplessample208
Known GenesRCAN3, RCAN3AS
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086819
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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