A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14316860



Internal ID22226361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185056646..185056646hg38UCSC Ensembl
chr4:185977800..185977800hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3563730
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14316860
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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