A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094819



Internal ID21285669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19277806..19355019hg38UCSC Ensembl
Innerchr4:19279429..19356642hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3877214
hg1977214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112208
Supporting Variants
Samplessample378
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094819
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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