A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092090



Internal ID21274501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:78774597..78778392hg38UCSC Ensembl
Innerchr4:79695751..79699546hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg383796
hg193796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112804
Supporting Variants
Samplessample208
Known GenesBMP2K
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092090
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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