A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14313155



Internal ID22256527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43757976..43757976hg38UCSC Ensembl
chr4:43759993..43759993hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3563773
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14313155
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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