A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095845



Internal ID21279492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55844255..55886491hg38UCSC Ensembl
Innerchr13:56418389..56460625hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3842237
hg1942237
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112584
Supporting Variants
Samplessample285
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095845
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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