A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14316420



Internal ID22210218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119993635..119993635hg38UCSC Ensembl
chr4:120914790..120914790hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3563677
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14316420
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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