A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14311961



Internal ID22168044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26316534..26316534hg38UCSC Ensembl
chr4:26318156..26318156hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3563561
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14311961
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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