A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098348



Internal ID21284249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25430432..25434801hg38UCSC Ensembl
Innerchr1:25756923..25761292hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384370
hg194370
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114211
Supporting Variants
Samplessample359
Known GenesTMEM57
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098348
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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