A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107702



Internal ID21283959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:73246043..73258599hg38UCSC Ensembl
Innerchr5:72541870..72554426hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3812557
hg1912557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112178
Supporting Variants
Samplessample353
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107702
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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