A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095872



Internal ID21280739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:52307527..52359753hg38UCSC Ensembl
Innerchr13:52881662..52933888hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3852227
hg1952227
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111038
Supporting Variants
Samplessample302
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095872
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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