A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093441



Internal ID21279989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5241483..5388317hg38UCSC Ensembl
Innerchr4:5243210..5390044hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38146835
hg19146835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110178
Supporting Variants
Samplessample291
Known GenesSTK32B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093441
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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