A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088620



Internal ID21275847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12499254..12516592hg38UCSC Ensembl
Innerchr10:12541253..12558591hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3817339
hg1917339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117058
Supporting Variants
Samplessample228
Known GenesCAMK1D
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088620
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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