A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098193



Internal ID21284042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26109733..26112817hg38UCSC Ensembl
Innerchr1:26436224..26439308hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383085
hg193085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114232
Supporting Variants
Samplessample357
Known GenesPDIK1L
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098193
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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