A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093624



Internal ID21282449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66517104..66527034hg38UCSC Ensembl
Innerchr4:67382822..67392752hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg389931
hg199931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110489
Supporting Variants
Samplessample327
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093624
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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